Abstract
Fungal diseases have been emerging as an important public health problem worldwide with the increase in host predisposition factors due to immunological dysregulations, immunosuppressive and/or anticancer therapy. Antifungal therapy for systemic mycosis is limited, most of times expensive and causes important toxic effects. Nanotechnology has become an interesting strategy to improve efficacy of traditional antifungal drugs, which allows lower toxicity, better biodistribution, and drug targeting, with promising results in vitro and in vivo. In this review, we provide a discussion about conventional antifungal and nanoantifungal therapies for systemic mycosis.
Keywords: antifungal therapy, fungal infection, mycosis, nanobiotechnology, drug delivery systems
Introduction
Fungal diseases have arisen as an important public health problem worldwide, having a great impact in human morbidity and mortality, specially among immunocompromised individuals (Denning and Hope, 2010; Shapiro et al., 2011; Caffrey and Obar, 2016; Prasad et al., 2016). Although superficial mycosis are the most common among fungal infections, affecting nearly 25% of the human population worldwide (Havlickova et al., 2008), invasive fungal infections are of greater concern, since they are life-threatening, difficult to diagnose and account with a limited number of therapeutic options (Brown et al., 2012a,b). It is estimated that systemic mycosis cause about 1.5 million deaths annually (Brown et al., 2012a; Caffrey and Obar, 2016).
Systemic fungal infections include both opportunistic and endemic mycosis, and are associated with high rates of mortality if not readily diagnosed and treated (Brown et al., 2012a; Caffrey and Obar, 2016). Opportunistic infections are caused by environmental or commensal fungi and affect immunocompromised or genetically predisposed hosts, accounting for about 2 million life-threatening reported cases each year worldwide (Brown et al., 2012a; Polvi et al., 2015; Caffrey and Obar, 2016). Species from genera Aspergillus, Candida, Cryptococcus, and Pneumocystis are responsible for more than 90% of all reported fungal-related deaths, although accurate incidence data is not officially available and may be underestimated (Brown et al., 2012a,b).
On the other hand, endemic mycoses are caused by thermal-dimorphic fungi and can affect especially immunocompetent hosts that live in particular geographic areas, although immunosuppression is a risk factor and contributes to the outcome of infection (Goughenour and Rappleye, 2017). Dimorphic fungi occur as saprophytic molds in the environment. After inhalation or trauma inoculation by the mammalian host, they transform into pathogenic yeasts or spherules (Bonifaz et al., 2011; Sil and Andrianopoulos, 2015). Among the causative agents of endemic mycosis are Histoplasma capsulatum, Coccidioides immitis and C. posadasii, Paracoccidioides brasiliensis, and P. lutzii, Blastomyces dermatitidis, Talaromyces marneffei, and Sporothrix schenckii. Despite incidence data of infections by dimorphic fungi are usually inaccurate due to under-diagnosis and under-reporting, it is believed that endemic mycosis are responsible for approximately 65,000 life-threatening cases each year worldwide (Brown et al., 2012a; Goughenour and Rappleye, 2017).
The fact that fungi and animals are evolutionarily close makes the search for therapeutic targets a big challenge, since targets such as biomolecules synthesis have great potential for toxicity (Groll et al., 1998; Denning and Hope, 2010; Heitman, 2011; Shapiro et al., 2011; Polvi et al., 2015). Today, only a dozen of antifungal agents (Table 1) are approved for the treatment of invasive fungal infections (Seyedmousavi et al., 2017). Antifungal therapy for systemic mycosis is basically focused in three classes: polyenes, azoles, and echinocandins (Polvi et al., 2015). Therapies for invasive infection presents restrictions such as route of administration, toxicity, drug interactions and sometimes high costs, considering patients hospitalization (Denning and Hope, 2010; Brown et al., 2012b; Polvi et al., 2015). In some cases, prolonged treatment times are needed, together with clinical interventions due to side effects (Goughenour and Rappleye, 2017). Recently, drug resistance has also become a worrisome issue (Xie et al., 2014). Unfortunately, antifungal drug development does not follow the progressive increase of invasive infections resulted from modern medical interventions, primary, and acquired immunodeficiencies and immunosuppressive therapies. Besides, there are no approved human vaccines for fungal diseases at this moment (Brown et al., 2012b). To overcome these problems, it is interesting to develop cheaper and novel therapeutic strategies in the battle against fungal diseases.
Table 1.
Antifungal spectrum | AMB | 5FC | FLU | ITR | VOR | POS | ISA | CAS | MIC | ANI |
---|---|---|---|---|---|---|---|---|---|---|
Candida albicans | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ |
Candida glabrata | ++ | ++ | + | + | ++ | ++ | ++ | + | + | + |
Candida parapsilosis | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ |
Candida tropicalis | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ |
Candida krusei | ++ | + | – | + | ++ | ++ | ++ | ++ | ++ | ++ |
Candida lusitaniae | – | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ | ++ |
Aspergillus fumigatus | ++ | – | – | + | ++ | ++ | ++ | + | + | + |
Cryptococcus neoformans | ++ | ++ | ++ | ++ | ++ | ++ | ++ | – | – | – |
Mucorales | ++ | – | – | – | – | ++ | ++ | – | – | – |
Fusarium spp. | + | – | – | + | ++ | ++ | ++ | – | – | – |
Scedosporium spp. | + | – | – | + | + | + | + | – | – | – |
Blastomyces dermatitidis | ++ | – | + | ++ | ++ | ++ | ++ | – | – | – |
Coccidioides immitis | ++ | – | ++ | ++ | ++ | ++ | ++ | – | – | – |
Histoplasma capsulatum | ++ | – | + | ++ | ++ | ++ | ++ | – | – | – |
Class | Polyene | Pyrimidine | Azole | Echinocandins | ||||||
Target | Ergosterol | Nucleic acid | Ergosterol | Cell wall | ||||||
Administration | Intravenous | Oral | Oral/Intravenous | Intravenous | ||||||
Side Effects | Infusion reactions, hepatotoxicity, nephrotoxicity | Bone marrow suppression, liver toxicity | Gastrointestinal upset, hepatotoxicity, liver failure | Infusion reactions, gastrointestinal upset, headache, liver toxicity |
5FC, flucytosine; AMB, amphotericin B; ANI, anidulafungin; CAS, caspofungin; FLU, fluconazole; ISA, isavuconazole; ITR, itraconazole; MIC, micafungin; POS, posaconazole; VOR, voriconazole.
Adapted from Nett and Andes (2016).
In this review, we will discuss current antifungal therapies available for systemic infections and point out some of the strategies using nanobiotechnology to improve conventional therapy. We will give a brief introduction about nanoformulations, and provide an overview of current studies proposing nanostructuration as an approach to improve efficacy and bioavailability of conventional antifungal drugs.
Conventional therapy for invasive fungal diseases
In the late 1950s, polyenes emerged as the first class of antifungal agents. These molecules are produced by Streptomyces nodosus presenting high affinity for ergosterol, the major sterol in fungal cell membrane, which is responsible for membrane fluidity, asymmetry, and integrity (Odds et al., 2003; Carrillo-Muñoz et al., 2006; Mesa-Arango et al., 2012). By binding to ergosterol, polyene molecules complex forming pores that destabilize cell membrane, allowing leakage of cellular contents and resulting in fungal cell death (Finkelstein and Holz, 1973; Georgopapadakou, 1998; Mesa-Arango et al., 2012; Adler-Moore et al., 2016). Besides, induction of oxidative damage in the fungal cell also contributes to fungicidal activity (Georgopapadakou, 1998; Mesa-Arango et al., 2012). Unluckily, polyene agents can also interact with cholesterol, what confers potential toxicity for mammalian cells (Hsuchen and Feingold, 1973; Georgopapadakou, 1998; Mesa-Arango et al., 2012). Among Polyenes, Amphotericin B is the most used for the treatment of systemic fungal infections. Amphotericin B has fungicidal effects against a broad-spectrum of fungal pathogens and is approved for the treatment of numerous invasive mycosis, such as candidiasis, aspergillosis, cryptococcosis, blastomycosis, histoplasmosis, mucormycosis, and sporotrichosis (Georgopapadakou, 1998; Mesa-Arango et al., 2012; Adler-Moore et al., 2016; Nett and Andes, 2016).
Amphotericin B was first introduced in the market in 1958 as a sodium deoxycholate solution administrated by parenteral route (Bartner et al., 1958; Groll et al., 1998), and after almost 60 years, it is still considered the gold standard for the treatment of most life-threatening mycosis (Groll et al., 1998; Carrillo-Muñoz et al., 2006; Mesa-Arango et al., 2012). However, this formulation is associated with important acute and chronic side-effects, particularly nephrotoxicity (Carrillo-Muñoz et al., 2006; Laniado-Laborín and Cabrales-Vargas, 2009; Mesa-Arango et al., 2012; Nett and Andes, 2016). Amphotericin B has the ability to stimulate proinflammatory responses, enhancing antifungal activity, although this may also be associated with toxicity (Mesa-Arango et al., 2012). In order to circumvent toxicity problems, lipid formulations were developed, including liposomes (Ambisome®), lipid complexes (Abelcet®), and colloidal dispersions (Amphocil®/Amphotech®) (Georgopapadakou, 1998; Gulati et al., 1998; Dupont, 2002; Mesa-Arango et al., 2012; Nett and Andes, 2016). However, these alternatives can be up to 20-fold more expensive than sodium deoxycholate Amphotericin B (Georgopapadakou, 1998; Wong-Beringer et al., 1998; Dismukes, 2000; Falci et al., 2011), limiting its usage in public health systems with limited resources.
In the late 1960s, flucytosine (5-fluorocytosine), a synthetic pyrimidine analog originally designed for antitumor therapy, was first used in the treatment of invasive mycosis (Tassel and Madoff, 1968). After being imported to the fungal cell by cytosine permeases, 5-fluorocytosine is converted to fluorouracil, which gets incorporated into DNA and RNA molecules during their synthesis, inhibiting protein synthesis and DNA replication, thus impairing cell function (Groll et al., 1998; Nett and Andes, 2016; Prasad et al., 2016). These agents have activity against a limited spectrum of pathogenic yeasts, such as C. albicans, C. glabrata, C. parapsilosis, C. tropicalis, and Cryptococcus spp., and are poor effective against dimorphic or filamentous fungi (Nett and Andes, 2016; Prasad et al., 2016). Due to rapid occurrence of resistance during the therapy with flucytosine, specially among Candida species, its clinical use is preferable only in combination with other antifungal drugs, such as Amphotericin B in the treatment of cryptococcal meningitis and other life-threatening Candida infections (Tassel and Madoff, 1968; Francis and Walsh, 1992; Dismukes, 2000; Sanglard et al., 2009; Nett and Andes, 2016; Prasad et al., 2016). Besides, Flucytosine induces significant side-effects, like liver dysfunction and bone marrow suppression (Francis and Walsh, 1992; Groll et al., 1998; Dismukes, 2000; Nett and Andes, 2016; Prasad et al., 2016). In the United States, flucytosine is available in oral capsules (Groll et al., 1998; Nett and Andes, 2016).
Azoles are synthetic cyclic organic molecules introduced in the early 1970s in addition to antifungal arsenal. They are composed by a 5-member azole ring, which contains two (imidazoles) or three (triazoles) nitrogen atoms, attached to a complex side chain (Georgopapadakou, 1998; Groll et al., 2003). Azoles target is ergosterol biosynthesis, which is impaired due to inhibition of fungi cytochrome P-450 14-α sterol demethylase (Vanden Bossche et al., 1995; Georgopapadakou, 1998; Groll et al., 1998, 2003; Odds et al., 2003; Carrillo-Muñoz et al., 2006). As a consequence, cell membrane integrity is impaired, with sterol precursors accumulation inside fungal cell and depletion of ergosterol in cell membrane, altering normal permeability and fluidity (Georgopapadakou, 1998; Groll et al., 1998; Odds et al., 2003). In general, azoles have a fungistatic action, affecting cell growth and proliferation, and eventually, due to accumulation of toxic methylated sterols, fungal cell death may occur (Groll et al., 2003; Zonios and Bennett, 2008; Sanglard et al., 2009; Arnold et al., 2010; Shapiro et al., 2011; Prasad et al., 2016). Currently, azoles are the most diverse class of antifungal agents and they have been refined during the past 40 years (Odds et al., 2003). Imidazoles emerged first (Groll et al., 1998; Prasad et al., 2016), and among them, miconazole and ketoconazole were the only available for systemic use (Groll et al., 2003), with the last being the first orally absorbable antifungal and the first alternative to Amphotericin B (Groll et al., 1998; Seyedmousavi et al., 2017). Triazoles came next, Itraconazole in oral formulations, and Fluconazole, in both oral and i.v. formulations, both better tolerated and more effective than Ketoconazole (Dismukes, 2000), with increased potency, expanded antifungal spectrum and improved resistance to metabolic degradation (Como and Dismukes, 1994; Groll et al., 1998). Fluconazole has good activity against Cryptococcus spp., Coccidioides spp., and Candida spp. except for C. krusei and C. glabrata (Arnold et al., 2010; Denning and Hope, 2010; Nett and Andes, 2016; Seyedmousavi et al., 2017). Itraconazole has broader antifungal spectrum, being effective against Candida spp., Cryptococcus neoformans, Aspergillus spp., dimorphic fungi, and dermatophytes (Arnold et al., 2010; Denning and Hope, 2010; Nett and Andes, 2016).
Further modifications in the molecules gave rise to the second generation of triazoles, in which Voriconazole (structurally related to Fluconazole) and Posaconazole (related to Itraconazole) are available for systemic therapy with even better antifungal potency and specificity. Voriconazole spectrum of activity is improved in relation to first generation triazoles, also including C. glabrata, Fusarium spp., Scedosporium spp. (Arnold et al., 2010; Denning and Hope, 2010; Nett and Andes, 2016). Posaconazole exhibits the widest antifungal spectrum of the azoles, being active against both yeasts and molds, including several Mucorales species (Arnold et al., 2010; Denning and Hope, 2010; Nett and Andes, 2016). Isavuconazole is the newest triazole introduced in the market in 2015 and recently approved for the treatment of invasive aspergillosis and mucormycosis in the USA and Europe (McCormack, 2015).
Although azole antifungals are generally well-tolerated (Odds et al., 2003; Carrillo-Muñoz et al., 2006), they are substrates and inhibitors of several cytochrome P-450 enzymes, what is the mainly cause of their adverse effects, specially hepatotoxicity (Carrillo-Muñoz et al., 2006). For this reason, azoles can also impair metabolism of coadministered drugs, what leads to decreased plasma concentration and unexpected toxicity (Groll et al., 1998; Dismukes, 2000; Shapiro et al., 2011; Nett and Andes, 2016; Prasad et al., 2016). Besides, due to teratogenic effects, azoles are contraindicated during pregnancy (Arnold et al., 2010; Nett and Andes, 2016). Lastly, the emergence of resistance among fungal isolates is another limitation and one of the motivations for the improvement of this class of antifungals (Dismukes, 2000; Shapiro et al., 2011; Prasad et al., 2016).
Echinocandins are the newest category of antifungals agents, consisting in fungi derived semisynthetic lipopeptides composed of a cyclic hexapeptide core and a variable lipid side chain responsible for their antifungal activity (Groll et al., 2003; Odds et al., 2003). Although they were discovered in the 1970s, only 30 years later their use was approved by the US Food and Drug Administration. Echinocandins inhibits the synthesis of 1,3-β-glucan, a structural fungal cell wall polysaccharide that is responsible for cell wall's shape and rigidity, osmotic integrity and is important in cell division and cell growth (Georgopapadakou, 2001; Groll et al., 2003; Odds et al., 2003). Echinocandins includes caspofungin, anidulafungin and micafungin, all of them only available for i.v. administration (Groll et al., 2003; Odds et al., 2003). Their effect is species-dependent, acting as fungicidal against Candida spp. and fungistatic against Aspergillus spp. (Nett and Andes, 2016), with variable activity against dematiaceous and endemic mold (Seyedmousavi et al., 2017). However, echinocandins have no activity against Scedosporium spp., Fusarium spp., and C. neoformans (Groll et al., 2003; Odds et al., 2003; Arnold et al., 2010; Nett and Andes, 2016). Since echinocandins target β-glucan, which is not present in the mammalian cell, they present minimal side effects in humans (Groll et al., 2003; Sanglard et al., 2009; Arnold et al., 2010; Shapiro et al., 2011; Prasad et al., 2016), which may include gastrointestinal upsets headache and increased liver aminotransferases. Few drug-drug interactions were reported since echinocandins are not metabolized through cytochrome P-450 enzymes (Arnold et al., 2010; Nett and Andes, 2016).
As stated above, although antifungal arsenal currently available for systemic mycoses is effective against the majority of fungal pathogens, they present limitations such as toxicity, drug-drug interactions, and emergence of clinical resistance. In order to overcome these problems, strategies like combination therapy (Mukherjee et al., 2005) and even repurposing of established medications (Butts and Krysan, 2012) are being exploited. The search for new compounds and new targets, together with the improvement of existing formulations are extremely needed. Nanostructuration of conventional antifungal agents may be an interesting alternative to achieve a better antifungal efficacy and safety (Figure 1).
Nanobiotechnological approaches for antifungal delivery
Drug delivery systems containing nanoparticles have been object of intense investigation for the past decades, becoming an efficient strategy to increase drug bioavailability, reduce toxicity and enhance antifungal potency (Vyas and Gupta, 2006; Amaral and Felipe, 2013; de Sá et al., 2015; Stiufiuc et al., 2015). Among the advantages of this approach is the possibility to build formulations for a smart delivery, for example, targeting specific tissues and organs, such as the lungs, which are frequently the initial infection site during systemic fungal diseases (Amaral et al., 2009; Malathi and Balasubramanian, 2011; Moritz and Geszke-Moritz, 2015). In some cases, during intracellular infections, nanoparticles can penetrate the cells, leading the drug to act directly against the pathogen (Borborema et al., 2011; Dube et al., 2014). On the other hand, when coated with substances such as polyethylene glycol (PEG), they can evade recognition by the phagocytic system, preventing the attachment of opsonines, and promoting a longer circulation time (Stiufiuc et al., 2015). Studies have shown that nanoparticles also have desirable characteristics to be used as adjuvants in vaccines (Van Slooten et al., 2001; Agger et al., 2008; Bhowmick et al., 2008; Ribeiro et al., 2013). Currently, many types of nanostructures are under investigation for drug delivery of antifungal drugs, such as polymeric nanoparticles, solid lipid nanoparticles, liposomes, and magnetic nanoparticles (Figure 2).
Polymeric nanoparticles are prepared from various natural or synthetic polymers, both hydrophilic and hydrophobic (Pagels and Prud'homme, 2015). These polymers may be of natural origin, such as chitosan and alginate, or synthetics, such as poly (lactic acid, PLA) and poly (glycolic acid, PGA) or a combination of both forming the poly (lactide-co-glycolide acid, PLGA) (Bolhassani et al., 2014). When applied in vivo, polymeric nanoparticles suffer biodegradation to be metabolized and excreted by the organism, what confers better biocompatibility (Amaral and Felipe, 2013). As the polymer is degraded, the drug incorporated within is released to the medium and can efficiently reach the site of action.
Liposomes are particles made by natural or synthetic phospholipids. Because of the nature of these molecules, when in contact with an aqueous medium, they form spherical structures containing an aqueous nucleus surrounded by a lipid bilayer (Bozzuto and Molinari, 2015), which can be suitable for delivery of both hydrophilic and hydrophobic substances (Stiufiuc et al., 2015). Because of their sensitivity to pH variations, liposomes permeability can be adjusted, releasing the drug into specific sites, such as macrophage compartments with altered pH during an infection (Wang et al., 2014; Jiang et al., 2015). A successful example of this class of nanoparticles is the commercially available liposomal Amphotericin B, brand name Ambisome® (Reis, 2015). In addition, solid lipid nanoparticles have been intensively investigated, specially for topical drug delivery (Kumar and Sinha, 2016; Trombino et al., 2016). They are spherical nanoparticles constituted of physiological and biodegradable lipids, such as stearic acid. Due to chemical composition, solid lipid nanoparticles allow the nanostructuration of insoluble drugs, and have low toxicity.
Magnetic nanoparticles have received special attention for biological applications, mainly because of their ability to be manipulated by a magnetic field, so that it can be directed and delivered to, theoretically, a specific site of the organism (Hussein et al., 2014). This type of nanoparticles can be prepared by different chemical and physical methodologies using ferrous compounds such as cobalt, manganese and zinc ferrites, magnetite, and maghemite. In the medical field, these magnetic nanoparticles are mainly used for clinical diagnosis through magnetic resonance imaging (MRI). This type of nanoparticle can also be associated with other nanostructures, such as polymeric nanoparticles or liposomes, to combine characteristics for both MRI and drug delivery (Jain et al., 2008). The superparamagnetic iron oxide nanoparticles, a specific kind of magnetic nanoparticle, respond more efficiently to an external magnetic field (Kumar et al., 2010) presenting a great potential to be used as drug carriers.
There are over a 100 publications proposing new nanoformulations for antifungal drugs (Table 2). In this review, we will summarize the major findings for nanoparticles that had proven in vivo and/ or in vitro antifungal activity.
Table 2.
Antifungal agent | Type Of nanoparticle | Administration | In vivo | In vitro | References |
---|---|---|---|---|---|
Amphotericin B | Lipid nanoparticles | Inhalation | N/A | Candida albicans, Cryptococcus neoformans | Gangadhar et al., 2014 |
Intravenous | Aspergillus fumigatus | Candida albicans, Aspergillus fumigatus | Jung et al., 2009 | ||
Intravenous | Aspergillus fumigatus | N/A | Sheikh et al., 2010 | ||
Intravenous | Candida albicans | N/A | Burgess et al., 2013 | ||
Liposomes | N/A | N/A | Candida albicans, Candida tropicalis | Albasarah et al., 2010 | |
Magnetic nanoparticles | Nasal instilation | Paracoccidioides brasiliensis | N/A | Saldanha et al., 2016 | |
Nanoemulsion | Topical | N/A | Aspergillus fumigatus, Aspergilus niger, Candida albicans | Hussain et al., 2016 | |
Nanosuspension | Ocular | N/A | Fusarium solani | Das and Suresh, 2011 | |
Polymeric nanoparticles | Inhalation | Aspergillus fumigatus | N/A | Shirkhani et al., 2015 | |
Intraperitoneal | Aspergillus fumigatus | N/A | Van de Ven et al., 2012 | ||
Intraperitoneal | Paracoccidioides brasiliensis | N/A | Amaral et al., 2009; Souza et al., 2015 | ||
Intravenous | Candida albicans | N/A | Tang et al., 2014, 2015a | ||
Intravenous | Candida glabrata | N/A | Tang et al., 2015b | ||
Intravenous | Cryptococcus neoformans | N/A | Xu et al., 2011 | ||
Intravenous | N/A | Candida albicans | Han et al., 2007 | ||
Intravenous | Candida albicans | Zia et al., 2015 | |||
N/A | Candida glabrata | N/A | Tang et al., 2015c | ||
N/A | N/A | Candida albicans | Tiyaboonchai et al., 2001; Tang et al., 2014 | ||
N/A | N/A | Candida albicans, Candida tropicalis | Casa et al., 2015 | ||
Ocular | N/A | Candida albicans | Zhou et al., 2013 | ||
Ocular | N/A | Candida albicans, Aspergillus fumigatus | Zhou et al., 2013 | ||
Oral | Candida albicans, Aspergillus fumigatus | N/A | Serrano et al., 2015 | ||
Polymeric nanoparticles | Oral/intravenous | Aspergillus fumigatus | N/A | Italia et al., 2011 | |
Topical | Candida albicans, Candida glabrata, Candida parapsilosis | N/A | Sanchez et al., 2014 | ||
Solid Lipid Nanoparticles | N/A | N/A | Candida albicans | Vieira and Carmona-Ribeiro, 2008 | |
Oral | N/A | Candida albicans | Chaudhari et al., 2016 | ||
Amphotericin B and Nystatin | Magnetic nanoparticles | N/A | N/A | Candida albicans | Niemirowicz et al., 2016 |
Fluconazole | Polymeric nanoparticles | Ocular | Candida albicans | N/A | Rençber et al., 2016 |
Solid Lipid Nanoparticles | N/A | N/A | Candida albicans, Candida glabrata, Candida parapsilosis | Moazeni et al., 2016 | |
Topical | Candida albicans | N/A | Gupta and Vyas, 2012 | ||
Itraconazole | Lipid nanoparticles | Inhalation | Aspergillus fumigatus | N/A | Pardeike et al., 2016 |
Polymeric nanoparticles | N/A | Candida albicans | N/A | Qiu et al., 2015 | |
N/A | N/A | Aspergillus flavus | Patel et al., 2011 | ||
N/A | N/A | Candida albicans, Aspergillus fumigatus | Essa et al., 2012 | ||
N/A | N/A | Paracoccidioides brasiliensis | Cunha-Azevedo et al., 2011 | ||
N/A | N/A | Aspergillus flavus | Patel et al., 2010 | ||
Solid Lipid Nanoparticles | Ocular | N/A | Aspergillus flavus | Mohanty et al., 2015 | |
Miconazole | Liposomes | Topical | Candida albicans | N/A | Pandit et al., 2014 |
Solid Lipid Nanoparticles | Topical | Candida albicans | N/A | Jain et al., 2010 | |
Nystatin | Polymeric nanoparticles | N/A | N/A | Candida albicans | Mohammadi et al., 2017 |
Voriconazole | Polymeric nanoparticles | Oral | Candida albicans | N/A | Peng et al., 2008 |
Nanopreparations for polyenes
Among antifungal drugs, the investigation surrounding nanostructured delivery systems for polyenes are the most reported, the majority of them concerning Amphotericin B delivery. This is not surprising, since Amphotericin B is still the gold standard for antifungal therapy of severe systemic mycosis and the drug with the most potent antifungal capacity (Arnold et al., 2010). Amphotericin B nanoparticles have been investigated since 1980s, providing the opportunity to circumvent infusion-related side effects and nephrotoxicity, which are the main limiting factors concerning therapy with this drug. Further, because of the Amphotericin B poor solubility and oral bioavailability (Kang et al., 2010), such formulations are also intended to improve these characteristics, making it suitable for oral delivery.
Currently, lipid formulations for Amphotericin B are commercially available (Walsh et al., 1999; Kleinberg, 2006). The most successful is Ambisome®, which is considered a truly liposomal formulation, where Amphotericin B is embedded in the unilamellar liposome bilayer of about 45–80 nm (Adler-Moore, 1994). One of the advantages brought by this formulation is that it causes less toxicity and remains at high peaks in the circulation, presenting in a high biodistribution. A study using the murine model of pulmonary aspergillosis showed that Ambisome® was able to increase the survival of animals without toxicity, allowing the administration of a 10-fold higher dose than in animals receiving the conventional formulation in sodium deoxycholate (Takemoto, 2006). Liposomal formulations for topical applications have also been explored (Kang et al., 2010; Perez et al., 2016). Some of these preparations aim to increase the permanency of the formulation at the site of action, releasing the drug for longer time. Unfortunately, together with the higher biosafety, it was reported that antifungal effectiveness of Amphotericin B lipid formulations may be reduced in comparison to that of free drug (Andes et al., 2006; Burgess et al., 2013). In addition to that, the high costs are among the limitations to their widespread use (Dismukes, 2000; Falci et al., 2011; Italia et al., 2011; Van de Ven et al., 2012), encouraging the search for new options for Amphotericin B delivery.
In order to diminish costs of manufacturing, Nanosomal Amphotericin B was developed using phosphatidylcholine and sodium cholesteryl sulfate as excipients avoiding the use of organic solvents or detergents in the preparation (Sheikh et al., 2010). Nanosomal Amphotericin B induced less lysis of red blood cells than Amphotericin B sodium deoxycholate and was comparable to Ambisome®. No symptoms of toxicity, mortality or significant body weight reduction were observed in rabbits daily treated with this formulation for 28 days, with no hematological and gross pathological abnormalities. Besides, in mice disseminated A. fumigatus infection, intravenous administration of Nanosomal Amphotericin B resulted in 90% survival while only 30% survival with Ambisome®.
Anionic and PEG lipid nanoparticles were developed by Jung et al. (2009) for intravenous delivery of Amphotericin B (Jung et al., 2009). This formulation presented lower cytotoxicity against human kidney cells than Fungizone® and Ambisome®, and much lower hematotoxicity than that of Fungizone®. Antifungal activity in vitro of Amphotericin B lipid nanoparticles against C. albicans and A. fumigatus was better than the commercialized formulations and in vivo administration for the treatment of murine systemic aspergilloma was more effective than that of Ambisome®.
Burgess et al. (2013) developed a formulation consisting of a protein-phospholipid bioparticle (NanoDisk) containing a “super aggregate” form of amphotericin B (ND–AMB) (Burgess et al., 2013). ND–AMB presented lower C. albicans and A. fumigatus minimum inhibitory concentrations than those observed for Ambisome®. It also induced no kidney or liver toxicity in mice. In addition, in C. albicans infected immune-competent mice, ND-AMB treatment was as effective as sodium deoxycholate amphotericin B or Ambisome®, whereas in a leukopenic model of candidiasis, the 50% effective dose of ND-AMB was around threefold lower than Ambisome®.
In addition to the lipid formulations, polymeric systems for the delivery of Amphotericin B have been developed by several research groups (Table 2). The results proved this type of preparation to be satisfactory for the efficient delivery of this drug by several routes, such as intravenously (Amaral et al., 2009; Tang et al., 2014; Souza et al., 2015) and orally (Italia et al., 2009, 2011, 2012). The biological response may vary according to the type of polymer used or even by combining different polymer types. An example is the formulation developed by Tang et al. (2014), in which AMB was encapsulated within PLGA in association with ε-caprolactone. In this combination, the authors reported an AMB encapsulation efficiency of 84% and the same fungicidal effect on C. albicans as for the free drug (Tang et al., 2014). The proposed formulation was less toxic and caused lower mortality than free AMB, proving, as noted before, the potential of polymeric nanoparticles to protect against cytotoxicity but preserving the same fungicidal efficacy (Amaral et al., 2009).
Amaral et al. (2009) developed a nanostructured formulation for Amphotericin B within PLGA functionalized with dimercaptosuccinic acid (DMSA). This acid presents tropism to the lungs, being suitable to be incorporation in formulations for drug delivery to this organ (Amaral et al., 2009, 2010). In this study, authors noted that intraperitoneal administration of the formulation was able to cause the same therapeutic effect in murine model of paracoccidioidomycosis compared to sodium deoxycholate Amphotericin B. However, the great advantage of this polymeric formulation was that it was given to the animals every 3 days, considering the slow release of Amphotericin B from nanoparticles, in contrast to the conventional formulation, which was administrated daily. Complementary studies conducted by the same research group showed that amphotericin B PLGA nanoparticles were also comparable to Ambisome® in the therapy of murine paracoccidioidomycosis (Souza et al., 2015). In addition, both studies reported no undesirable side effects in animals at the dose used. High concentrations of Amphotericin B were found in lungs, liver and spleen of animals treated with this polymeric formulation (Souza et al., 2015).
Van de Ven et al. (2012) showed that both Amphotericin B PLGA nanoparticles and nanoemulsion had in vitro antifungal capacity against C. albicans, A. fumigatus, and Trichophyton rubrum and were less hemolytic than sodium deoxycholate Amphotericin B (Van de Ven et al., 2012). In addition, both formulations were effective against murine disseminated aspergillosis after intraperitoneal administration, with similar or even better antifungal capacity than Fungizone® and Ambisome® at equivalent doses. Italia et al. (2011) proposed Amphotericin B PLGA nanoparticles for oral delivery, which significantly reduced fungal burden during invasive pulmonary and disseminated aspergillosis (Italia et al., 2011).
In a very interesting approach, Tang et al. (2015a) developed specialized pH-responsive Amphotericin B PLGA nanoparticles conjugated with poly(L-histidine) and PEG that had high affinity for fungal cell wall elements under acidic conditions and were further modified for increased targeting efficacy with anti-C. albicans antibody (Tang et al., 2015a). The formulation had reduced hemolytic activity and cytotoxicity on human renal tubular epithelial cells, and was effective against C. albicans both in vivo and in vitro after intravenous administration. Nystatin loaded PLGA nanoparticles functionalized with Glucosamine were formulated by Mohammadi et al. (2017) to enhance the adhesion of nanoparticles to C. albicans cell walls (Mohammadi et al., 2017). The nanoparticles exhibited higher antifungal activity than free Nystatin, suggesting an increase in Nystatin levels in fungal cell membrane by entrapment in the polymeric matrix.
Chitosan is a natural polysaccharide with cationic nature and mucoadhesive proprieties that has been frequently used to build biodegradable polymeric nanoparticles for drug delivery. Amphotericin B chitosan nanoparticles were developed by Serrano et al. (2015) intending to avoid drug gastrointestinal degradation, improve stability and enhance bioavailability in target organs such as lung, liver, and spleen, while diminishing kidney exposure (Serrano et al., 2015). They have demonstrated that oral administration of these nanoparticles was effective in the treatment of murine models of visceral leishmaniasis, candidiasis and aspergillosis, having comparable efficacy to parenteral Ambisome®. Chitosan nanoparticles were used by Sanchez et al. (2014) for topical delivery of Amphotericin B to burn wounds infected with C. albicans, with enhanced tissue healing and even better antifungal activity than sodium deoxycholate formulation (Sanchez et al., 2014). Amphotericin B loaded nanoparticles made of lecithin and chitosan were proposed by Chhonker et al. (2015) for prolonged ocular application such as during fungal keratitis (Chhonker et al., 2015). The formulation presented in vitro antifungal efficacy against C. albicans and A. fumigatus, pronounced mucoadhesive properties and improved bioavailablity as compared with Fungizone®.
Approaches to increase Amphotericin B delivery into central nervous system (CNS) are also under investigation. Amphotericin B polybutylcyanoacrylate nanoparticles modified with polysorbate 80 were used as therapy for cryptococcal meningitis murine model (Xu et al., 2011). Nanoparticles were detected in the brain 30 min after systemic administration into mice with a higher concentration than Amphotericin B liposomes. Survival rate of mice treated with nanoparticles was significantly higher than that of sodium deoxycholate and liposomal amphotericin B treated groups, with lower fungal burden in brain tissue. Another formulation based in transferrin transcytosis at the blood-brain barrier was proposed by Tang et al. (2015c). In this study, anti-transferrin receptor antibody-modified Amphotericin B-loaded PLA-PEG nanoparticles were developed and presented significant reduction of CNS fungal burden and increased mouse survival time when administered intravenously for the treatment of meningitis induced by C. glabrata inoculation (Tang et al., 2015c).
Shirkhani et al. (2015) developed Amphotericin B polymethacrylic acid nanoparticles for the prophylaxis of A. fumigatus infection in a transplant immunosuppression murine model with invasive aspergillosis. The formulation was given by nebulization and prevented fungal growth and lung inflammation (Shirkhani et al., 2015).
Amphotericin B magnetic nanoparticles were reported by Saldanha et al. (2016). In this study, authors developed Amphotericin B loaded lauric acid pre-coated magnetite nanoparticles and showed nanocomplex antifungal activity both in vivo and in vitro against P. brasiliensis infection (Saldanha et al., 2016). The nanocomplex was more cytotoxic to fungal cells than to human urinary cells and murine peritoneal macrophages in vitro, while no biochemical and histopathological alterations were observed during intranasal therapy against murine paracoccidioidomycosis. The formulation exhibited similar antifungal activity to that of sodium deoxycholate Amphotericin B administrated intraperitonealy, with the advantage to allow a three-fold reduction in the number of applications and to be suitable for nasal delivery. Another Amphotericin B magnetic liposomal system were proposed by Zhao et al. (2014) aiming to enhance drug selectivity to CNS during fungal infections. The liposomal system was administered via carotid artery route in SD rats and could improve drug concentration and enhance magnetic targeting to brain tissue in the presence of a magnetic field. Amphotericin B and nystatin magnetic nanoparticles were also designed by Niemirowicz et al. (2016). Both nanosystems displayed stronger fungicidal activity than unbound drugs against Candida spp. (Niemirowicz et al., 2016). Nanosystems were more potent than free agents when tested against Candida strains and were able to prevent Candida biofilm formation more effectively with lower hemolytic capacity.
Some fungal pathogens have the ability to reside inside host cells, such as macrophages. Therefore, nanoparticles uptake by host cells is very desirable as a strategy to enhance antifungal abilities against intracellular fungi. Zia et al. (2015) showed that killing of intracellular C. albicans after treatment with amphotericin B polyglutamic acid nanoparticles was higher than with Ambisome® (Zia et al., 2015). Amphotericin B is also used for the treatment of infections caused by Leishmania spp., which is an intracellular parasite, so that intense investigation has been done in order to enhance drug antiparasitic effects throughout nanostruturation (Asthana et al., 2015; Jain et al., 2015; Bose et al., 2016).
Nanopreparations for azoles
The increase of oral bioavailability of azoles is one of the advantages conferred by the use of nanotechnology for this class of drug. It is interesting to note that although preparing a formulation at the nanoscale may suggest similar results when using the same type of nanoparticle and material, this is not always true. For example, a study encapsulating econazole and clotrimazole in both PLGA and alginate (Pandey et al., 2005) demonstrated that the latter seems to be better at improving pharmacokinetic parameters. Though, both proved to be effective for the oral route.
Considering the severity of some fungal infections affecting the lungs, nanostructured delivery systems for drugs capable of reaching this organ are sought. Some studies showed the tropism for the lungs by PLGA nanoparticles. The PLGA-encapsulated voriconazole showed a higher accumulation in the lungs when compared with free voriconazole (Das et al., 2015). This characteristic was also observed by other researchers when they also encapsulated voriconazole in PLGA for nasal administration. The study demonstrated the system allows the early release of the drug in the lungs in the first 2 h, followed by a sustained release during 15 days (Sinha et al., 2013). Itraconazole PLGA nanoparticles conjugated with dimercaptosuccinic acid were developed for pulmonary delivery and induced antifungal inhibition against P. brasiliensis with lower in vitro cytotoxicity than free drug (Cunha-Azevedo et al., 2011).
Voriconazole loaded PLGA nanoparticles were developed by Peng et al. (2008) in order to improve drug bioavailability and stability for oral delivery (Peng et al., 2008). Nanoparticles had a more persistent and potent antifungal effect than free voriconazole both in vitro and in vivo in a systemic candidiasis murine model.
Other triazole loaded polymeric nanostructured formulations have been investigated and had in vitro antifungal activities against A. flavus (Patel et al., 2010, 2011), A. fumigatus (Essa et al., 2012), and C. albicans (Qiu et al., 2015). Some polymers have mucoadhesive properties, such as chitosan, and can be used to prepare drug delivery systems for mucosa from the eyes, mouth and vagina. Rençber et al. (2016) developed a buccal mucoadhesive nanoparticle containing fluconazole and EUDRAGIT®, a nonbiodegradable and cationic copolymer, for the local treatment of oral candidiasis. The formulation presented in vitro antifungal activity against C. albicans for an extended period, and no cytotoxic effect in chinese hamster ovary cells was observed. Rabbits with oral candidiasis were successfully treated with local administration of the nanoparticles once a day (Rençber et al., 2016). More sophisticated drug delivery systems formed by different types of nanoparticles can be prepared (Jøraholmen et al., 2014). For example, in one polymer the drug is encapsulated and this polymer is coated with another to present the proper in vivo application.
Ultraflexible liposomes carrying miconazole also showed to be more efficient and able to penetrate the cell barrier carrying the drug. As they are able to adapt their shape according to the characteristics of the near microenvironment, they are able to penetrate and release the drug more efficiently (Pandit et al., 2014). It is also possible to promote the release of miconazole only to the skin, without penetrating it or reaching the epidermis (Elmoslemany et al., 2012), which is important for reducing toxicity.
Solid lipid nanoparticles (SLN) have been intensively investigated for topical delivery of azole antifungals. Jain et al. (2010) developed a formulation of miconazole nitrate loaded SLN-bearing hydrogel for skin delivery (Jain et al., 2010). Studies indicated that miconazole SLN-bearing hydrogel resulted in considerably less skin irritation as compared to miconazole hydrogel and suspension after 24 h of application. In addition, micozanole SLN treatment of cutaneous candidiasis in albino rats presented greater efficiency and fast recovery. Mohanty et al. (2015) investigated SLNs for topical ocular delivery of itraconazole (Mohanty et al., 2015). Permeation of itraconazole in freshly excised goat corneas was observed, and SLN inhibited Aspergillus flavus in vitro growth, indicating antimicrobial efficacy of formulations.
Moazeni et al. (2016) tested fluconazole-loaded SLN efficacy against fluconazole-resistant Candida spp. strains. Fluconazole-resistant C. albicans, C. parapsilosis, and C. glabrata strains behaved as susceptible strains after treatment with fluconazole SLN, emphasizing the promising benefits of nanostructuration for the delivery of antifungal agents.
Concluding remarks
The high incidence of fungal infections is a problem that can be aggravated mainly by the increase of the elderly population and also by immunocompromised patients. In this way, it is important that new and more effective therapies are developed for the treatment of these mycoses. One strategy that has received importance for this purpose is the development of drugs applying the principles of nanotechnology. It is possible to use the same conventional drugs, but aiming to increase its therapeutic efficacy and also the reduction of its side effects. Thus, unlike the basic development of a novel antifungal molecule, which is also of relevant importance, conventional formulations may be improved in effectiveness by the resources of Nanobiotechnology.
Author contributions
All authors listed, have made substantial, direct and intellectual contribution to the work, and approved it for publication.
Funding
Ana Camila Oliveira Souza is funded by grant 2015/10390-6 from the Fundação de Amparo à Pesquisa de São Paulo (FAPESP).
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
- Adler-Moore J. (1994). AmBisome targeting to fungal infections. Bone Marrow Transplant. 14(Suppl. 5), S3–S7. [PubMed] [Google Scholar]
- Adler-Moore J. P., Gangneux J. P., Pappas P. G. (2016). Comparison between liposomal formulations of amphotericin B. Med. Mycol. 54, 223–231. 10.1093/mmy/myv111 [DOI] [PubMed] [Google Scholar]
- Agger E. M., Rosenkrands I., Hansen J., Brahimi K., Vandahl B. S., Aagaard C., et al. (2008). Cationic liposomes formulated with synthetic mycobacterial cordfactor (CAF01): a versatile adjuvant for vaccines with different immunological requirements. PLoS ONE 3:e3116. 10.1371/journal.pone.0003116 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Albasarah Y. Y., Somavarapu S., Stapleton P., Taylor K. M. (2010). Chitosan-coated antifungal formulations for nebulisation. J. Pharm. Pharmacol. 62, 821–828. 10.1211/jpp.62.05.0002 [DOI] [PubMed] [Google Scholar]
- Amaral A. C., Bocca A. L., Ribeiro A. M., Nunes J., Peixoto D. L., Simioni A. R., et al. (2009). Amphotericin B in poly(lactic-co-glycolic acid) (PLGA) and dimercaptosuccinic acid (DMSA) nanoparticles against paracoccidioidomycosis. J. Antimicrob. Chemother. 63, 526–533. 10.1093/jac/dkn539 [DOI] [PubMed] [Google Scholar]
- Amaral A. C., Felipe M. S. S. (2013). Nanobiotechnology: an efficient approach to drug delivery of unstable biomolecules. Curr. Protein Pept. Sci. 14, 588–594. 10.2174/1389203711209070632 [DOI] [PubMed] [Google Scholar]
- Amaral A. C., Marques A. F., Muñoz J. E., Bocca A. L., Simioni A. R., Tedesco A. C., et al. (2010). Poly(lactic acid-glycolic acid) nanoparticles markedly improve immunological protection provided by peptide P10 against murine paracoccidioidomycosis. Br. J. Pharmacol. 159, 1126–1132. 10.1111/j.1476-5381.2009.00617.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- Andes D., Safdar N., Marchillo K., Conklin R. (2006). Pharmacokinetic-pharmacodynamic comparison of amphotericin B (AMB) and two lipid-associated AMB preparations, liposomal AMB and AMB lipid complex, in murine candidiasis models. Antimicrob. Agents Chemother. 50, 674–684. 10.1128/AAC.50.2.674-684.2006 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Arnold T. M., Dotson E., Sarosi G. A., Hage C. A. (2010). Traditional and emerging antifungal therapies. Proc. Am. Thorac. Soc. 7, 222–228. 10.1513/pats.200906-048AL [DOI] [PubMed] [Google Scholar]
- Asthana S., Gupta P. K., Jaiswal A. K., Dube A., Chourasia M. K. (2015). Overexpressed macrophage mannose receptor targeted nanocapsules- mediated cargo delivery approach for eradication of resident parasite: in vitro and in vivo studies. Pharm. Res. 32, 2663–2677. 10.1007/s11095-015-1651-0 [DOI] [PubMed] [Google Scholar]
- Bartner E., Zinnes H., Moe R. A., Kuleska J. S. (1958). Studies on a new solubilized preparation of amphotericin B. Antibiot. Annu. 5, 53–58. [PubMed] [Google Scholar]
- Bhowmick S., Ravindran R., Ali N. (2008). gp63 in stable cationic liposomes confers sustained vaccine immunity to susceptible BALB/c mice infected with Leishmania donovani. Infect. Immun. 76, 1003–1015. 10.1128/IAI.00611-07 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bolhassani A., Javanzad S., Saleh T., Hashemi M., Aghasadeghi M. R., Sadat S. M. (2014). Polymeric nanoparticles. Hum. Vaccin. Immunother. 10, 321–332. 10.4161/hv.26796 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bonifaz A., Vázquez-González D., Perusquía-Ortiz A. M. (2011). Endemic systemic mycoses: coccidioidomycosis, histoplasmosis, paracoccidioidomycosis and blastomycosis. J. Dtsch. Dermatol. Ges. 9, 705–715. 10.1111/j.1610-0387.2011.07731.x [DOI] [PubMed] [Google Scholar]
- Borborema S. E., Schwendener R. A., Osso J. A., de Andrade H. F., Jr., do Nascimento N. (2011). Uptake and antileishmanial activity of meglumine antimoniate-containing liposomes in Leishmania (Leishmania) major-infected macrophages. Int. J. Antimicrob. Agents 38, 341–347. 10.1016/j.ijantimicag.2011.05.012 [DOI] [PubMed] [Google Scholar]
- Bose P. P., Kumar P., Dwivedi M. K. (2016). Hemoglobin guided nanocarrier for specific delivery of amphotericin B to Leishmania infected macrophage. Acta Trop. 158, 148–159. 10.1016/j.actatropica.2016.02.026 [DOI] [PubMed] [Google Scholar]
- Bozzuto G., Molinari A. (2015). Liposomes as nanomedical devices. Int. J. Nanomedicine 10, 975–999. 10.2147/IJN.S68861 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown G. D., Denning D. W., Gow N. A., Levitz S. M., Netea M. G., White T. C. (2012a). Hidden killers: human fungal infections. Sci. Transl. Med. 4, 165rv13. 10.1126/scitranslmed.3004404 [DOI] [PubMed] [Google Scholar]
- Brown G. D., Denning D. W., Levitz S. M. (2012b). Tackling human fungal infections. Science 336, 647–647. 10.1126/science.1222236 [DOI] [PubMed] [Google Scholar]
- Burgess B. L., He Y., Baker M. M., Luo B., Carroll S. F., Forte T. M., et al. (2013). NanoDisk containing super aggregated amphotericin B: a high therapeutic index antifungal formulation with enhanced potency. Int. J. Nanomedicine 8, 4733–4743. 10.2147/IJN.S50113 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Butts A., Krysan D. J. (2012). Antifungal drug discovery: something old and something new. PLoS Pathog. 8:e1002870. 10.1371/journal.ppat.1002870 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Caffrey A. K., Obar J. J. (2016). Alarmin(g) the innate immune system to invasive fungal infections. Curr. Opin. Microbiol. 32, 135–143. 10.1016/j.mib.2016.06.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carrillo-Muñoz A. J., Giusiano G., Ezkurra P. A., Quindós G. (2006). Antifungal agents: mode of action in yeast cells. Rev. Esp. Quimioter. 19, 130–139. [PubMed] [Google Scholar]
- Casa D. M., Carraro T. C., de Camargo L. E., Dalmolin L. F., Khalil N. M., Mainardes R. M. (2015). Poly(L-lactide) nanoparticles reduce amphotericin B cytotoxicity and maintain its in vitro antifungal activity. J. Nanosci. Nanotechnol. 15, 848–854. 10.1166/jnn.2015.9177 [DOI] [PubMed] [Google Scholar]
- Chaudhari M. B., Desai P. P., Patel P. A., Patravale V. B. (2016). Solid lipid nanoparticles of amphotericin B (AmbiOnp): in vitro and in vivo assessment towards safe and effective oral treatment module. Drug Deliv. Transl. Res. 6, 354–364. 10.1007/s13346-015-0267-6 [DOI] [PubMed] [Google Scholar]
- Chhonker Y. S., Prasad Y. D., Chandasana H., Vishvkarma A., Mitra K., Shukla P. K., et al. (2015). Amphotericin-B entrapped lecithin/chitosan nanoparticles for prolonged ocular application. Int. J. Biol. Macromol. 72, 1451–1458. 10.1016/j.ijbiomac.2014.10.014 [DOI] [PubMed] [Google Scholar]
- Como J. A., Dismukes W. E. (1994). Oral azole drugs as systemic antifungal therapy. N. Engl. J. Med. 330, 263–272. 10.1056/NEJM199401273300407 [DOI] [PubMed] [Google Scholar]
- Cunha-Azevedo E. P., Silva J. R., Martins O. P., Siqueira-Moura M. P., Bocca A. L., Felipe M. S., et al. (2011). In vitro antifungal activity and toxicity of itraconazole in DMSA-PLGA nanoparticles. J. Nanosci. Nanotechnol. 11, 2308–2314. 10.1166/jnn.2011.3576 [DOI] [PubMed] [Google Scholar]
- Das P. J., Paul P., Mukherjee B., Mazumder B., Mondal L., Baishya R., et al. (2015). Pulmonary delivery of voriconazole loaded nanoparticles providing a prolonged drug level in lungs: a promise for treating fungal infection. Mol. Pharm. 12, 2651–2664. 10.1021/acs.molpharmaceut.5b00064 [DOI] [PubMed] [Google Scholar]
- Das S., Suresh P. K. (2011). Nanosuspension: a new vehicle for the improvement of the delivery of drugs to the ocular surface. Application to amphotericin B. Nanomedicine 7, 242–247. 10.1016/j.nano.2010.07.003 [DOI] [PubMed] [Google Scholar]
- Denning D. W., Hope W. W. (2010). Therapy for fungal diseases: opportunities and priorities. Trends Microbiol. 18, 195–204. 10.1016/j.tim.2010.02.004 [DOI] [PubMed] [Google Scholar]
- de Sá F. A., Taveira S. F., Gelfuso G. M., Lima E. M., Gratieri T. (2015). Liposomal voriconazole (VOR) formulation for improved ocular delivery. Colloids Surf. B Biointerfaces 133, 331–338. 10.1016/j.colsurfb.2015.06.036 [DOI] [PubMed] [Google Scholar]
- Dismukes W. E. (2000). Introduction to antifungal drugs. Clin. Infect. Dis. 30, 653–657. 10.1086/313748 [DOI] [PubMed] [Google Scholar]
- Dube A., Reynolds J. L., Law W.-C., Maponga C. C., Prasad P. N., Morse G. D. (2014). Multimodal nanoparticles that provide immunomodulation and intracellular drug delivery for infectious diseases. Nanomedicine 10, 831–838. 10.1016/j.nano.2013.11.012 [DOI] [PubMed] [Google Scholar]
- Dupont B. (2002). Overview of the lipid formulations of amphotericin B. J. Antimicrob. Chemother. 49(Suppl. 1), 31–36. 10.1093/jac/49.suppl_1.31 [DOI] [PubMed] [Google Scholar]
- Elmoslemany R. M., Abdallah O. Y., El-Khordagui L. K., Khalafallah N. M. (2012). Propylene glycol liposomes as a topical delivery system for miconazole nitrate: comparison with conventional liposomes. AAPS PharmSciTech 13, 723–731. 10.1208/s12249-012-9783-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Essa S., Louhichi F., Raymond M., Hildgen P. (2012). Improved antifungal activity of itraconazole-loaded PEG/PLA nanoparticles. J. Microencapsul. 30, 1–13. 10.3109/02652048.2012.714410 [DOI] [PubMed] [Google Scholar]
- Falci D. R., dos Santos R. P., Wirth F., Goldani L. Z. (2011). Continuous infusion of amphotericin B deoxycholate: an innovative, low-cost strategy in antifungal treatment. Mycoses 54, 91–98. 10.1111/j.1439-0507.2009.01805.x [DOI] [PubMed] [Google Scholar]
- Finkelstein A., Holz R. (1973). Aqueous pores created in thin lipid membranes by the polyene antibiotics nystatin and amphotericin B. Membranes (Basel). 2, 377–408. [PubMed] [Google Scholar]
- Francis P., Walsh T. J. (1992). Evolving role of flucytosine in immunocompromised patients: new insights into safety, pharmacokinetics, and antifungal therapy. Clin. Infect. Dis. 15, 1003–1018. [DOI] [PubMed] [Google Scholar]
- Gangadhar K. N., Adhikari K., Srichana T. (2014). Synthesis and evaluation of sodium deoxycholate sulfate as a lipid drug carrier to enhance the solubility, stability and safety of an amphotericin B inhalation formulation. Int. J. Pharm. 471, 430–438. 10.1016/j.ijpharm.2014.05.066 [DOI] [PubMed] [Google Scholar]
- Georgopapadakou N. H. (1998). Antifungals: mechanism of action and resistance, established and novel drugs. Curr. Opin. Microbiol. 1, 547–557. 10.1016/S1369-5274(98)80087-8 [DOI] [PubMed] [Google Scholar]
- Georgopapadakou N. H. (2001). Update on antifungals targeted to the cell wall: focus on β-1,3-glucan synthase inhibitors. Expert Opin. Investig. Drugs 10, 269–280. 10.1517/13543784.10.2.269 [DOI] [PubMed] [Google Scholar]
- Goughenour K. D., Rappleye C. A. (2017). Antifungal therapeutics for dimorphic fungal pathogens. Virulence 8, 211–221. 10.1080/21505594.2016.1235653 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Groll A. H., Gea-Banacloche J. C., Glasmacher A., Just-Nuebling G., Maschmeyer G., Walsh T. J. (2003). Clinical pharmacology of antifungal compounds. Infect. Dis. Clin. North Am. 17, 159–191. 10.1016/S0891-5520(02)00068-5 [DOI] [PubMed] [Google Scholar]
- Groll A. H., Piscitelli S. C., Walsh T. J. (1998). Clinical pharmacology of systemic antifungal agents: a comprehensive review of agents in clinical use, current investigational compounds, and putative targets for antifungal drug development. Adv. Pharmacol. 44, 343–500. 10.1016/S1054-3589(08)60129-5 [DOI] [PubMed] [Google Scholar]
- Gulati M., Bajad S., Singh S., Ferdous A. J., Singh M. (1998). Development of liposomal amphotericin B formulation. J. Microencapsul. 15, 137–151. 10.3109/02652049809006844 [DOI] [PubMed] [Google Scholar]
- Gupta M., Vyas S. P. (2012). Development, characterization and in vivo assessment of effective lipidic nanoparticles for dermal delivery of fluconazole against cutaneous candidiasis. Chem. Phys. Lipids 165, 454–461. 10.1016/j.chemphyslip.2012.01.006 [DOI] [PubMed] [Google Scholar]
- Han K., Miah M. A. J., Shanmugam S., Yong C. S., Choi H.-G., Kim J. A., et al. (2007). Mixed micellar nanoparticle of amphotericin B and poly styrene-block-poly ethylene oxide reduces nephrotoxicity but retains antifungal activity. Arch. Pharm. Res. 30, 1344–1349. 10.1007/BF02980276 [DOI] [PubMed] [Google Scholar]
- Havlickova B., Czaika V. A., Friedrich M. (2008). Epidemiological trends in skin mycoses worldwide. Mycoses 51, 2–15. 10.1111/j.1439-0507.2008.01606.x [DOI] [PubMed] [Google Scholar]
- Heitman J. (2011). Microbial pathogens in the fungal kingdom. Fungal Biol. Rev. 25, 48–60. 10.1016/j.fbr.2011.01.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hsuchen C. C., Feingold D. S. (1973). Selective membrane toxicity of the polyene antibiotics: studies on natural membranes. Antimicrob. Agents Chemother. 4, 316–319. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hussain A., Samad A., Singh S. K., Ahsan M. N., Haque M. W., Faruk A., et al. (2016). Nanoemulsion gel-based topical delivery of an antifungal drug: in vitro activity and in vivo evaluation. Drug Deliv. 23, 642–647. 10.3109/10717544.2014.933284 [DOI] [PubMed] [Google Scholar]
- Hussein M. Z., Al Ali S., Geilich B. M., El Zowalaty M. E., Webster T. J. (2014). Synthesis, characterization, and antimicrobial activity of an ampicillin-conjugated magnetic nanoantibiotic for medical applications. Int. J. Nanomedicine 9, 3801–3814. 10.2147/IJN.S61143 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Italia J. L., Kumar M. N. V. R., Carter K. C. (2012). Evaluating the potential of polyester nanoparticles for per oral delivery of amphotericin B in treating visceral leishmaniasis. J. Biomed. Nanotechnol. 8, 695–702. 10.1166/jbn.2012.1414 [DOI] [PubMed] [Google Scholar]
- Italia J. L., Sharp A., Carter K. C., Warn P., Kumar M. N. (2011). Peroral amphotericin B polymer nanoparticles lead to comparable or superior in vivo antifungal activity to that of intravenous Ambisome® or Fungizone™. PLoS ONE 6:e25744. 10.1371/journal.pone.0025744 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Italia J. L., Yahya M. M., Singh D., Ravi Kumar M. N. (2009). Biodegradable nanoparticles improve oral bioavailability of amphotericin B and show reduced nephrotoxicity compared to intravenous fungizone®. Pharm. Res. 26, 1324–1331. 10.1007/s11095-009-9841-2 [DOI] [PubMed] [Google Scholar]
- Jain K., Verma A. K., Mishra P. R., Jain N. K. (2015). Characterization and evaluation of amphotericin B loaded MDP conjugated poly(propylene imine) dendrimers. Nanomedicine 11, 705–713. 10.1016/j.nano.2014.11.008 [DOI] [PubMed] [Google Scholar]
- Jain S., Jain S., Khare P., Gulbake A., Bansal D., Jain S. K. (2010). Design and development of solid lipid nanoparticles for topical delivery of an anti-fungal agent. Drug Deliv. 17, 443–451. 10.3109/10717544.2010.483252 [DOI] [PubMed] [Google Scholar]
- Jain T. K., Richey J., Strand M., Leslie-Pelecky D. L., Flask C. A., Labhasetwar V. (2008). Magnetic nanoparticles with dual functional properties: drug delivery and magnetic resonance imaging. Biomaterials 29, 4012–4021. 10.1016/j.biomaterials.2008.07.004 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jiang L., Li L., He X., Yi Q., He B., Cao J., et al. (2015). Overcoming drug-resistant lung cancer by paclitaxel loaded dual-functional liposomes with mitochondria targeting and pH-response. Biomaterials 52, 126–139. 10.1016/j.biomaterials.2015.02.004 [DOI] [PubMed] [Google Scholar]
- Jøraholmen M. W., Vanić Z., Tho I., Skalko-Basnet N. (2014). Chitosan-coated liposomes for topical vaginal therapy: assuring localized drug effect. Int. J. Pharm. 472, 94–101. 10.1016/j.ijpharm.2014.06.016 [DOI] [PubMed] [Google Scholar]
- Jung S. H., Lim D. H., Jung S. H., Lee J. E., Jeong K.-S., Seong H., et al. (2009). Amphotericin B-entrapping lipid nanoparticles and their in vitro and in vivo characteristics. Eur. J. Pharm. Sci. 37, 313–320. 10.1016/j.ejps.2009.02.021 [DOI] [PubMed] [Google Scholar]
- Kang J.-W., Davaa E., Kim Y.-T., Park J.-S. (2010). A new vaginal delivery system of amphotericin B: a dispersion of cationic liposomes in a thermosensitive gel. J. Drug Target. 18, 637–644. 10.3109/10611861003649712 [DOI] [PubMed] [Google Scholar]
- Kleinberg M. (2006). What is the current and future status of conventional amphotericin B? Int. J. Antimicrob. Agents 27(Suppl. 1), 12–16. 10.1016/j.ijantimicag.2006.03.013 [DOI] [PubMed] [Google Scholar]
- Kumar A., Jena P. K., Behera S., Lockey R. F., Mohapatra S., Mohapatra S. (2010). Multifunctional magnetic nanoparticles for targeted delivery. Nanomedicine 6, 64–69. 10.1016/j.nano.2009.04.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kumar R., Sinha V. R. (2016). Solid lipid nanoparticle: an efficient carrier for improved ocular permeation of voriconazole. Drug Dev. Ind. Pharm. 42, 1956–1967. 10.1080/03639045.2016.1185437 [DOI] [PubMed] [Google Scholar]
- Laniado-Laborín R., Cabrales-Vargas M. N. (2009). Amphotericin B: side effects and toxicity. Rev. Iberoam. Micol. 26, 223–227. 10.1016/j.riam.2009.06.003 [DOI] [PubMed] [Google Scholar]
- Malathi S., Balasubramanian S. (2011). Synthesis of biodegradable polymeric nanoparticles and their controlled drug delivery for tuberculosis. J. Biomed. Nanotechnol. 7, 150–151. 10.1166/jbn.2011.1244 [DOI] [PubMed] [Google Scholar]
- McCormack P. L. (2015). Isavuconazonium: first global approval. Drugs 75, 817–822. 10.1007/s40265-015-0398-6 [DOI] [PubMed] [Google Scholar]
- Mesa-Arango A. C., Scorzoni L., Zaragoza O. (2012). It only takes one to do many jobs: amphotericin B as antifungal and immunomodulatory drug. Front. Microbiol. 3:286. 10.3389/fmicb.2012.00286 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moazeni M., Kelidari H. R., Saeedi M., Morteza-Semnani K., Nabili M., Gohar A. A., et al. (2016). Time to overcome fluconazole resistant Candida isolates: solid lipid nanoparticles as a novel antifungal drug delivery system. Colloids Surf. B Biointerfaces 142, 400–407. 10.1016/j.colsurfb.2016.03.013 [DOI] [PubMed] [Google Scholar]
- Mohammadi G., Shakeri A., Fattahi A., Mohammadi P., Mikaeili A., Aliabadi A., et al. (2017). Preparation, physicochemical characterization and anti-fungal evaluation of nystatin-loaded PLGA-glucosamine nanoparticles. Pharm. Res. 34, 301–309. 10.1007/s11095-016-2062-6 [DOI] [PubMed] [Google Scholar]
- Mohanty B., Majumdar D. K., Mishra S. K., Panda A. K., Patnaik S. (2015). Development and characterization of itraconazole-loaded solid lipid nanoparticles for ocular delivery. Pharm. Dev. Technol. 20, 458–464. 10.3109/10837450.2014.882935 [DOI] [PubMed] [Google Scholar]
- Moritz M., Geszke-Moritz M. (2015). Recent developments in application of polymeric nanoparticles as drug carriers. Adv. Clin. Exp. Med. 24, 749–758. 10.17219/acem/31802 [DOI] [PubMed] [Google Scholar]
- Mukherjee P. K., Sheehan D. J., Hitchcock C. A., Ghannoum M. A. (2005). Combination treatment of invasive fungal infections. Clin. Microbiol. Rev. 18, 163–194. 10.1128/CMR.18.1.163-194.2005 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nett J. E., Andes D. R. (2016). Antifungal agents: spectrum of activity, pharmacology, and clinical indications. Infect. Dis. Clin. North Am. 30, 51–83. 10.1016/j.idc.2015.10.012 [DOI] [PubMed] [Google Scholar]
- Niemirowicz K., Durnaś B., Tokajuk G., Głuszek K., Wilczewska A. Z., Misztalewska I., et al. (2016). Magnetic nanoparticles as a drug delivery system that enhance fungicidal activity of polyene antibiotics. Nanomedicine 12, 2395–2404. 10.1016/j.nano.2016.07.006 [DOI] [PubMed] [Google Scholar]
- Odds F. C., Brown A. J., Gow N. A. R. (2003). Antifungal agents: mechanisms of action. Trends Microbiol. 11, 272–279. 10.1016/S0966-842X(03)00117-3 [DOI] [PubMed] [Google Scholar]
- Pagels R. F., Prud'homme R. K. (2015). Polymeric nanoparticles and microparticles for the delivery of peptides, biologics, and soluble therapeutics. J. Control. Release 219, 519–535. 10.1016/j.jconrel.2015.09.001 [DOI] [PubMed] [Google Scholar]
- Pandey R., Ahmad Z., Sharma S., Khuller G. K. (2005). Nano-encapsulation of azole antifungals: potential applications to improve oral drug delivery. Int. J. Pharm. 301, 268–276. 10.1016/j.ijpharm.2005.05.027 [DOI] [PubMed] [Google Scholar]
- Pandit J., Garg M., Jain N. K. (2014). Miconazole nitrate bearing ultraflexible liposomes for the treatment of fungal infection. J. Liposome Res. 24, 163–169. 10.3109/08982104.2013.871025 [DOI] [PubMed] [Google Scholar]
- Pardeike J., Weber S., Zarfl H. P., Pagitz M., Zimmer A. (2016). Itraconazole-loaded nanostructured lipid carriers (NLC) for pulmonary treatment of aspergillosis in falcons. Eur. J. Pharm. Biopharm. 108, 269–276. 10.1016/j.ejpb.2016.07.018 [DOI] [PubMed] [Google Scholar]
- Patel N. R., Damann K., Leonardi C., Sabliov C. M. (2010). Itraconazole-loaded poly(lactic-co-glycolic) acid nanoparticles for improved antifungal activity. Nanomedicine (Lond). 5, 1037–1050. 10.2217/nnm.10.68 [DOI] [PubMed] [Google Scholar]
- Patel N. R., Damann K., Leonardi C., Sabliov C. M. (2011). Size dependency of PLGA-nanoparticle uptake and antifungal activity against Aspergillus flavus. Nanomedicine (Lond). 6, 1381–1395. 10.2217/nnm.11.35 [DOI] [PubMed] [Google Scholar]
- Peng H. S., Liu X. J., Lv G. X., Sun B., Kong Q. F., Zhai D. X., et al. (2008). Voriconazole into PLGA nanoparticles: improving agglomeration and antifungal efficacy. Int. J. Pharm. 352, 29–35. 10.1016/j.ijpharm.2007.10.009 [DOI] [PubMed] [Google Scholar]
- Perez A. P., Altube M. J., Schilrreff P., Apezteguia G., Celes F. S., Zacchino S., et al. (2016). Topical amphotericin B in ultradeformable liposomes: formulation, skin penetration study, antifungal and antileishmanial activity in vitro. Colloids Surf. B Biointerfaces 139, 190–198. 10.1016/j.colsurfb.2015.12.003 [DOI] [PubMed] [Google Scholar]
- Polvi E. J., Li X., O'Meara T. R., Leach M. D., Cowen L. E. (2015). Opportunistic yeast pathogens: reservoirs, virulence mechanisms, and therapeutic strategies. Cell. Mol. Life Sci. 72, 2261–2287. 10.1007/s00018-015-1860-z [DOI] [PMC free article] [PubMed] [Google Scholar]
- Prasad R., Shah A. H., Rawal M. K. (2016). Antifungals: Mechanism of Action and Drug Resistance, in Yeast Membrane Transporter Advances in Experimental Medicine and Biology, eds Ramos J., Sychrová H., Kschischo M. (Cham: Springer International Publishing; ), 327–349. [DOI] [PubMed] [Google Scholar]
- Qiu L., Hu B., Chen H., Li S., Hu Y., Zheng Y., et al. (2015). Antifungal efficacy of itraconazole-loaded TPGS-b-(PCL-ran-PGA) nanoparticles. Int. J. Nanomedicine 10, 1415–1423. 10.2147/IJN.S71616 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reis J. (2015). Liposomal formulations of amphotericin B : differences according to the scientific evidence. Rev. Esp. Quimioter. 28, 275–281. [PubMed] [Google Scholar]
- Rençber S., Karavana S. Y., Yılmaz F. F., Eraç B., Nenni M., Özbal S., et al. (2016). Development, characterization, and in vivo assessment of mucoadhesive nanoparticles containing fluconazole for the local treatment of oral candidiasis. Int. J. Nanomedicine 11, 2641–2653. 10.2147/IJN.S103762 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ribeiro A. M., Souza A. C. O., Amaral A. C., Vasconcelos N. M., Jeronimo M. S., Carneiro F. P., et al. (2013). Nanobiotechnological approaches to delivery of DNA vaccine against fungal infection. J. Biomed. Nanotechnol. 9, 221–230. 10.1166/jbn.2013.1491 [DOI] [PubMed] [Google Scholar]
- Saldanha C. A., Garcia M. P., Iocca D. C., Rebelo L. G., Souza A. C. O., Bocca A. L., et al. (2016). Antifungal activity of amphotericin B conjugated to nanosized magnetite in the treatment of paracoccidioidomycosis. PLoS Negl. Trop. Dis. 10:e0004754. 10.1371/journal.pntd.0004754 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sanchez D. A., Schairer D., Tuckman-Vernon C., Chouake J., Kutner A., Makdisi J., et al. (2014). Amphotericin B releasing nanoparticle topical treatment of Candida spp. in the setting of a burn wound. Nanomedicine 10, 269–277. 10.1016/j.nano.2013.06.002 [DOI] [PubMed] [Google Scholar]
- Sanglard D., Coste A., Ferrari S. (2009). Antifungal drug resistance mechanisms in fungal pathogens from the perspective of transcriptional gene regulation. FEMS Yeast Res. 9, 1029–1050. 10.1111/j.1567-1364.2009.00578.x [DOI] [PubMed] [Google Scholar]
- Serrano D. R., Lalatsa A., Dea-Ayuela M. A., Bilbao-Ramos P. E., Garrett N. L., Moger J., et al. (2015). Oral particle uptake and organ targeting drives the activity of amphotericin B nanoparticles. Mol. Pharm. 12, 420–431. 10.1021/mp500527x [DOI] [PubMed] [Google Scholar]
- Seyedmousavi S., Rafati H., Ilkit M., Tolooe A., Hedayati M. T., Verweij P. (2017). Systemic Antifungal Agents: Current Status and Projected Future Developments, in Methods in Molecular Biology, ed Lion T. (New York, NY: Springer New York; ), 107–139. [DOI] [PubMed] [Google Scholar]
- Shapiro R. S., Robbins N., Cowen L. E. (2011). Regulatory circuitry governing fungal development, drug resistance, and disease. Microbiol. Mol. Biol. Rev. 75, 213–267. 10.1128/MMBR.00045-10 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sheikh S., Ali S. M., Ahmad M. U., Ahmad A., Mushtaq M., Paithankar M., et al. (2010). Nanosomal amphotericin B is an efficacious alternative to ambisome for fungal therapy. Int. J. Pharm. 397, 103–108. 10.1016/j.ijpharm.2010.07.003 [DOI] [PubMed] [Google Scholar]
- Shirkhani K., Teo I., Armstrong-James D., Shaunak S. (2015). Nebulised amphotericin B-polymethacrylic acid nanoparticle prophylaxis prevents invasive aspergillosis. Nanomedicine 11, 1217–1226. 10.1016/j.nano.2015.02.012 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sil A., Andrianopoulos A. (2015). Thermally dimorphic human fungal pathogens–polyphyletic pathogens with a convergent pathogenicity trait. Cold Spring Harb. Perspect. Med. 5:a019794. 10.1101/cshperspect.a019794 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sinha B., Mukherjee B., Pattnaik G. (2013). Poly-lactide-co-glycolide nanoparticles containing voriconazole for pulmonary delivery: in vitro and in vivo study. Nanomedicine 9, 94–104. 10.1016/j.nano.2012.04.005 [DOI] [PubMed] [Google Scholar]
- Souza A. C. O., Nascimento A. L., de Vasconcelos N. M., Jerônimo M. S., Siqueira I. M., Santos R-L., et al. (2015). Activity and in vivo tracking of Amphotericin B loaded PLGA nanoparticles. Eur. J. Med. Chem. 95, 267–276. 10.1016/j.ejmech.2015.03.022 [DOI] [PubMed] [Google Scholar]
- Stiufiuc R., Iacovita C., Stiufiuc G., Florea A., Achim M., Lucaciu C. M. (2015). A new class of pegylated plasmonic liposomes: synthesis and characterization. J. Colloid Interface Sci. 437, 17–23. 10.1016/j.jcis.2014.09.023 [DOI] [PubMed] [Google Scholar]
- Takemoto K. (2006). Comparative study on the efficacy of AmBisome and Fungizone in a mouse model of pulmonary aspergillosis. J. Antimicrob. Chemother. 57, 724–731. 10.1093/jac/dkl005 [DOI] [PubMed] [Google Scholar]
- Tang X., Dai J., Xie J., Zhu Y., Zhu M., Wang Z., et al. (2015a). Enhanced Antifungal Activity by Ab-Modified Amphotericin B-Loaded Nanoparticles Using a pH-Responsive Block Copolymer. Nanoscale Res. Lett. 10:969. 10.1186/s11671-015-0969-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tang X., Jiao R., Xie C., Xu L., Huo Z., Dai J., et al. (2015b). Improved antifungal activity of amphotericin B-loaded TPGS-b-(PCL-ran-PGA) nanoparticles. Int. J. Clin. Exp. Med. 8, 5150–5162. 10.1016/j.ijbiomac.2014.10.014 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tang X., Liang Y., Zhu Y., Xie C., Yao A., Chen L., et al. (2015c). Anti-transferrin receptor-modified amphotericin B-loaded PLA-PEG nanoparticles cure Candidal meningitis and reduce drug toxicity. Int. J. Nanomedicine 10, 6227–6241. 10.2147/IJN.S84656 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tang X., Zhu H., Sun L., Hou W., Cai S., Zhang R., et al. (2014). Enhanced antifungal effects of amphotericin B-TPGS-b-(PCL-ran-PGA) nanoparticles in vitro and in vivo. Int. J. Nanomedicine 9:5403. 10.2147/IJN.S71623 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tassel D., Madoff M. A. (1968). Treatment of Candida sepsis and Cryptococcus meningitis with 5-fluorocytosine. A new antifungal agent. JAMA 206, 830–832. [PubMed] [Google Scholar]
- Tiyaboonchai W., Woiszwillo J., Middaugh C. R. (2001). Formulation and characterization of amphotericin B-polyethylenimine-dextran sulfate nanoparticles. J. Pharm. Sci. 90, 902–914. 10.1002/jps.1042 [DOI] [PubMed] [Google Scholar]
- Trombino S., Mellace S., Cassano R. (2016). Solid lipid nanoparticles for antifungal drugs delivery for topical applications. Ther. Deliv. 7, 639–647. 10.4155/tde-2016-0040 [DOI] [PubMed] [Google Scholar]
- Vanden Bossche H., Koymans L., Moereels H. (1995). P450 inhibitors of use in medical treatment: focus on mechanisms of action. Pharmacol. Ther. 67, 79–100. [DOI] [PubMed] [Google Scholar]
- Van de Ven H., Paulussen C., Feijens P. B., Matheeussen A., Rombaut P., Kayaert P., et al. (2012). PLGA nanoparticles and nanosuspensions with amphotericin B: potent in vitro and in vivo alternatives to Fungizone and AmBisome. J. Control. Release 161, 795–803. 10.1016/j.jconrel.2012.05.037 [DOI] [PubMed] [Google Scholar]
- Van Slooten M. L., Boerman O., Romøren K., Kedar E., Crommelin D. J., Storm G. (2001). Liposomes as sustained release system for human interferon-gamma: biopharmaceutical aspects. Biochim. Biophys. Acta 1530, 134–145. 10.1016/S1388-1981(00)00174-8 [DOI] [PubMed] [Google Scholar]
- Vieira D. B., Carmona-Ribeiro A. M. (2008). Cationic nanoparticles for delivery of amphotericin B: preparation, characterization and activity in vitro. J. Nanobiotechnology 6:6. 10.1186/1477-3155-6-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vyas S. P., Gupta S. (2006). Optimizing efficacy of amphotericin B through nanomodification. Int. J. Nanomedicine 1, 417–432. 10.2147/nano.2006.1.4.417 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walsh T. J., Finberg R. W., Arndt C., Hiemenz J., Schwartz C., Bodensteiner D., et al. (1999). Liposomal amphotericin B for empirical therapy in patients with persistent fever and neutropenia. National Institute of Allergy and Infectious Diseases Mycoses Study Group. N. Engl. J. Med. 340, 764–771. 10.1056/NEJM199903113401004 [DOI] [PubMed] [Google Scholar]
- Wang L., Geng D., Su H. (2014). Safe and efficient pH sensitive tumor targeting modified liposomes with minimal cytotoxicity. Colloids Surf. B Biointerfaces 123, 395–402. 10.1016/j.colsurfb.2014.09.003 [DOI] [PubMed] [Google Scholar]
- Wong-Beringer A., Jacobs R. A., Guglielmo B. J. (1998). Lipid formulations of amphotericin B: clinical efficacy and toxicities. Clin. Infect. Dis. 27, 603–618. 10.1086/514704 [DOI] [PubMed] [Google Scholar]
- Xie J. L., Polvi E. J., Shekhar-Guturja T., Cowen L. E. (2014). Elucidating drug resistance in human fungal pathogens. Future Microbiol. 9, 523–542. 10.2217/fmb.14.18 [DOI] [PubMed] [Google Scholar]
- Xu N., Gu J., Zhu Y., Wen H., Ren Q., Chen J. (2011). Efficacy of intravenous amphotericin B-polybutylcyanoacrylate nanoparticles against cryptococcal meningitis in mice. Int. J. Nanomedicine 6, 905–913. 10.2147/IJN.S17503 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhao M., Hu J., Zhang L., Zhang L., Sun Y., Ma N., et al. (2014). Study of amphotericin B magnetic liposomes for brain targeting. Int. J. Pharm. 475, 9–16. 10.1016/j.ijpharm.2014.08.035 [DOI] [PubMed] [Google Scholar]
- Zhou W., Wang Y., Jian J., Song S. (2013). Self-aggregated nanoparticles based on amphiphilic poly(lactic acid)-grafted-chitosan copolymer for ocular delivery of amphotericin B. Int. J. Nanomedicine 8, 3715–3728. 10.2147/IJN.S51186 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zia Q., Khan A. A., Swaleha Z., Owais M. (2015). Self-assembled amphotericin B-loaded polyglutamic acid nanoparticles: preparation, characterization and in vitro potential against Candida albicans. Int. J. Nanomedicine 10, 1769–1790. 10.2147/IJN.S63155 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zonios D. I., Bennett J. E. (2008). Update on azole antifungals. Semin. Respir. Crit. Care Med. 29, 198–210. 10.1055/s-2008-1063858 [DOI] [PubMed] [Google Scholar]