Exosome: A Review of Its Classification, Isolation Techniques, Storage, Diagnostic and Targeted Therapy Applications

Abstract

Exosomes are nano-sized small extracellular vesicles secreted by cells, carrying nucleic acids, proteins, lipids and other bioactive substances to play a role in the body’s physiological and pathological processes. Compared to synthetic carriers such as liposomes and nanoparticles, the endogeneity and heterogeneity of exosomes give them extensive and unique advantages in the field of disease diagnosis and treatment. However, the storage stability, low yield, low purity, and weak targeting of exosomes limit its clinical application. For this reason, further exploration is needed to optimize the above problems and facilitate future functional studies of exosomes. In this paper, the origin, classification, preparation and characterization, storage stability and applications of exosome delivery system are summarized and discussed by searching a large number of literatures.

Introduction

Exosomes, with a diameter of about 40–100nm, are biological nanoscale spherical lipid bilayer vesicles secreted by cells, floating at a density of 1.13–1.19 g ∙ mL⁻¹ in a sucrose density gradient solution.^1–5 In 1981, Trams et al⁶ collectively referred to plasma membrane-derived vesicles as exosomes and first proposed the concept of “exosomes”, which was regarded as membrane vesicles with 5‘-nucleotide enzyme activity that may have physiological functions and originate from the exudation of various cell line cultures. The currently defined exosomes (40–100nm) were first found in sheep reticulocytes in 1983.^7,8 Johnstone et al⁹ tracked transferrin receptors during the maturation of reticulocytes and found that the formation of exosomes is the mechanism for the loss of transferrin receptors in mature red blood cells. To distinguish them from other types of extracellular vesicles (EVs), they were named exosomes. However, it’s worth noting that the term “exosomes”, even if widely used, has been suggested to be replaced by the term “small Extracellular Vesicles (sEVs)” according to ISEV 2018 guidelines,¹⁰ due to methodological difficulties of separation. Studies have found that exosomes contain nucleic acids, proteins, lipids, cytokines, transcription factor receptors and other bioactive substances.^11,12 Among them, exosomal protein components are mainly divided into two categories, one is the public components, which participate in the process of vesicle formation and secretion, that is, exosomes are ubiquitous, including membrane transport and fusion-related proteins (like Rab, GTPases), Heat shock proteins (like HSP70, HSP90), four-transmembrane protein superfamily (like CD63,CD81), ESCRT complex-related proteins (like Tsg101, Alix), integrins, etc.; the other one is specific components, which are closely related to their progenitor cells, that is, cell-specific, such as CD45 and MHC-II derived from antigen-presenting cells. With the in-depth study of exosomes, its applications are becoming more and more widespread. Exosomes can play a role in physiological and pathological processes, acting as mediators for intercellular communication and material exchange. At the same time, exosomes can deliver a variety of bioactive substances and easy-to-deactivate or easily degradable ingredients (referring to therapeutic agents that have a short retention time in the body when administered alone) through multiple pathways and sites, and safely transfer them to target cells to participate in regulation, such as tissue repair, tumor diagnosis and treatment, and immune regulation.^5,13 In this review, we mainly focus on the classification, preparation and characterization of exosomes, storage stability, biomarkers, targeted drug delivery systems and provide some insights.

Origin and Classification of Exosomes

Formation

The initial endosomes are formed by the invagination of the cell membrane in the early stage, and then the bioactive substances begin to accumulate in the early sorting endosomes (ESEs). Then, under the control of the endocytosis sorting complex and other related proteins required for transport, the early endosomes become late sorting endosomes (LSEs). LSEs ultimately form multivesicular bodies (MVBs) after a second indentation. After MVBs fuses with the cell membrane, the substances inside the cells are released to the outside in the form of vesicles. These vesicles are exosomes. The biological origin of exosomes is shown in Figure 1. The formation of exosomes is diversified. At present, more researches are on ESCRT-dependent and ESCRT-independent mechanisms.^14–16 However, it has recently been reported that certain components, such as four-transmembrane domain proteins and lipid raft, are also involved in the formation of some exosomes.^17,18 Therefore, the exact mechanism remains controversial.

Figure 1.

Biogenesis of exosomes.

Classification

Exosomes are divided into natural exosomes and engineered exosomes based on whether they have been artificially modified. Ulteriorly, natural exosomes are divided into animal-derived exosomes and plant-derived exosomes. Because exosomes are produced under normal and tumor conditions, animal-derived exosomes are further divided into normal exosomes and tumor exosomes.

Almost all types of normal cells can produce exosomes, like human umbilical vein endothelial cells, mesenchymal stem cells (MSC), T cells, B cells, macrophages, dendritic cells (DC), natural killer (NK) cells.^19–22 For example, mesenchymal stem cells (MSCS) are pluripotent stem cells capable of self-renewal and multidirectional differentiation. MSCs can not only adapt to the tumor microenvironment, but also have powerful paracrine activity and secrete a large number of exosomes. Studies have demonstrated that paclitaxel (PTX) -containing exosomes have a significant inhibitory effect on the proliferation of the human pancreatic cancer cell line CFPAC-1 in vitro and have the potential to act as drug carriers.²³ In addition, MSC exosomes have been shown to play a role in the development of many diseases. They not only participate in the process of tissue repair and injury,^24,25 and have certain therapeutic effects on cardiovascular diseases (like myocardial infarction)^26,27 and neurological diseases,²⁸ but also can alleviate liver injury and be used in the treatment of liver diseases.²⁹ Macrophages are mononuclear phagocytes, which play a role in inflammation, immune regulation, wound healing, and angiogenesis.³⁰ Generally, macrophages are widely distributed in the body and can be polarized into M1 or M2 macrophages. Research has shown that macrophage-derived exosomes can affect the lung tissue microenvironment by affecting inflammatory signals and immune function.³¹ In additional, Exo-PTX has a significant anti-tumor effect in the Lewis lung cancer metastasis model. The macrophage-derived exosomes delivered via the respiratory pathway are almost completely co-located with the metastasis of cancer cells, which suggests that exosomes derived from macrophages may have specific surface proteins and tend to accumulate in the cancer cells preferentially, and the specific mechanism remains to be further investigated.³² Exosomes are able to inherit many specific biomolecules from parent cells, which is one of the reasons for their heterogeneity.³³ Not only that, there are some differences in the exosomes from different sources in terms of yield, contents, function, drug loading. As a result, different therapeutic effects may be produced. Kanchanapally et al³⁴ used co-incubation to successfully load doxorubicin (DOX) onto pancreatic stellate cells (PSCs), pancreatic cancer cells (PCCs) and macro-phage-derived exosomes. By contrast, exosomes derived from PSCs have the highest yield and high drug loading rate, while macrophage-derived exosomes have the strongest antitumor activity, indicating the specificity of exosomes from different sources.

Also, normal exosomes mentioned above can be widespread in biofluids, such as saliva, plasma, urine, ascites, milk and bile. Currently, milk-derived exosomes have been successfully developed to deliver the chemotherapeutic drug—paclitaxel, and the bioavailability, stability, safety and toxicity have been tested to meet standards.³⁵ Similarly, exosomes present in biofluids can express certain diagnostic and therapeutic properties. For example, in-depth study of circRNAs in exosomes present in blood or cerebrospinal fluid can contribute to reveal the underlying mechanisms of the development of neuropsychiatric disorders³⁶. Furthermore, miRNAs carried by serum exosomes can be used for the diagnosis and prognosis of spinal cord injury (SCI)³⁷. Likewise, by evaluating the expression profile of miRNAs in endometrial cancer (EC) and urine-derived exosomes from suspected patients, it was found that differentially expressed miRNAs can be used as biomarkers for EC diagnosis.³⁸

Tumor cells can secrete a large number of exosomes, and the specific antigens on their surface can reflect the nature of donor cells. Therefore, tumor exosomes have attracted great attention in cancer research. Tumor exosomes not only play an important role in the process of tumor growth, metastasis, and immune regulation,^39,40 but also monitor the development of diseases⁴¹ and serve as diagnostic markers for diseases.⁴² For example, Wu et al⁴³ found that colorectal cancer (CRC) cell-derived exosomes overexpressing CAPS1 can enhance the migration of normal colonic epithelial FHC cells. Therefore, inhibiting the secretion of tumor exosomes is a treatment option for patients with metastatic CRC. A study showed that TKIs are tyrosine kinase inhibitors targeting BCR-ABL1 p210 oncoprotein and have significant therapeutic effects on Philadelphia chromosome-positive chronic myeloid leukemia (Ph+ CML). The tumor exosomes in TKI-treated patients in the chronic phase of CML can identify the persistence of residual active leukemia cells which cannot be evaluated by the current standardized MRD monitoring system, and can be used as a new monitoring tool to prevent CML recurrence in the future.⁴¹

In addition, food-derived exosomes also have good development prospects. In recent years, studies have found that plant-derived exosome-like nanoparticles (ELN) have similar structures to mammalian exosomes. Ginger-derived particles can prevent the development of liver-related diseases, and ELN derived from grapes, carrots, grapefruit and ginger have anti-inflammatory effects and can maintain intestinal homeostasis.^44–47

At present, exosomes are classified mainly on the basis of sources. This classification does not analyze the characteristics and functional applications of various types of exosomes in detail. In the future, further subdivisions from the aspects of organophilicity, biological distribution and immunogenicity may be considered.²⁹

Preparation and Characterization

Isolation

With the in-depth study of exosomes, its potential application value has been continuously tapped. Reproducible isolation and enrichment of exosomes will help assess their biological functions. However, exosomes are heterogeneous in size, content, function and source,³³ which makes isolation difficult. Moreover, most current isolation technologies cannot completely separate exosomes from lipoproteins with similar biophysical characteristics and extracellular vesicles derived from non-endosomal pathways, resulting in low exosomal purity. Therefore, how to efficiently enrich exosomes is a major issue currently, which is crucial for downstream analysis of exosomes. For different purposes and applications, different isolation methods are selected, among which ultracentrifugation, size-based isolation techniques, polymer precipitation, immunoaffinity capture techniques are more commonly used.

Ultracentrifugation Techniques

Ultracentrifugation (UC) is currently the most widely used isolation technique and is also known as the gold standard for exosome extraction and separation. UC mainly harvests the required components based on the size and density differences of each component in the original solution, so it is suitable for the separation of large-dose sample components with significant differences in sedimentation coefficient.⁴⁸ Johnstone et al first applied this method to isolate exosomes in tissue culture medium of reticulocyte, and the method was optimized by Thery et al.^9,49 The ultracentrifugation is mainly divided into two steps: firstly, a series of continuous low-medium speed centrifugation to remove dead cells, cell debris and large-size extracellular vesicles, and then to separate exosomes at a higher speed with a centrifugal force of 100,000 × g, the exosomes were washed with PBS to remove impurities such as contaminating proteins. Studies have found that centrifugation time, centrifugal force, rotor type and parameters all affect the yield and purity of target exosomes.^48,50 This method does not need to label exosomes, which can avoid cross-contamination, but it is not conducive to downstream analysis due to its time consumption, high cost, structural damage, aggregation into blocks, and lipoprotein co-separation.^11,51

The purpose of density gradient centrifugation is to purify exosomes, and it is usually used in combination with ultracentrifugation to improve the purity of exosomes. There are two main types, one using sucrose as a medium, which is widely used in research. However, exosomes and retroviruses are extremely similar in terms of size and density, and the sucrose density gradient cannot effectively separate the two. At this point, Cantin et al.⁵² found that their sedimentation velocities in the iodixanol gradient is significantly different, which enabled the successful separation of exosomes from HIV-1-infected cells and the harvest of high-purity exosomes. In contrast, the density gradient centrifugation has an advantage in exosome purity, but the high viscosity of sucrose solution will reduce the sedimentation rate of exosomes, resulting in a longer time.⁵³

Polymer Precipitation

The method of polymer precipitation usually uses polyethylene glycol (PEG) as a medium, and the exosomes are harvested under the condition of centrifugation by reducing the solubility of the exosomes. This method was originally used to isolate viruses.⁵⁴ Because exosomes and viruses have similar biophysical characteristics, this method is often used in scientific research to isolate and purify exosomes. Rider et al.⁵⁵ compared three technologies of ultracentrifugation, modified polymer co-precipitation (ExtraPEG) and commercially available commercial kits, and found that the first two methods are better than the commercial method and that ExtraPEG is more cost effective, which surpasses ultracentrifugation in terms of purity and recovery. The polymer precipitation method is relatively easy to operate with short analysis time and is suitable for processing large doses of samples. However, the purity and recovery rate is relatively low and false positives may be generated, and the polymer produced is difficult to remove, which is not conducive to subsequent functional experimental analysis.

Size-Based Isolation Techniques

This technique mainly refers to ultrafiltration and size exclusion chromatography, which separates based on the size difference between exosomes and other components in biological samples.

The separation principle of size-exclusion chromatography (SEC) is that the macromolecules cannot enter the gel pores and that they are eluted along the gaps between the porous gels with the mobile phase, while the small molecules remain in the gel pores and are finally eluted by the mobile phase. At present, qEV separation columns, EVSecond purification columns, and Exo-spin exosome purification columns are commercially available based on the SEC principle. The application of SEC is quick, easy, and low-cost. The isolated exosomes have complete structure and uniform size, and their biological characteristics are not significantly adversely affected, but they may be doped with other particles of similar size, resulting in reduced purity.⁵¹

The method of ultrafiltration usually uses ultrafiltration membranes with different molecular weight cutoffs (MWCO) to selectively separate samples. The usage rate of this method is about 20%,⁵⁶ and it often plays a role in assisting separation in exosome research. The ultrafiltration method usually uses ultrafiltration tubes to separate exosomes with low cost and high enrichment efficiency and the activity of exosomes is not affected. However, there are problems with low purity and non-specific binding of exosomes and ultrafiltration membranes to reduce the recovery rate.⁵⁷

Immunoaffinity Chromatography (IAC)

Immunoaffinity chromatography is a separation and purification technology based on the specific binding of antibodies and ligands to separate desired substances from heterogeneous mixtures. The binding efficiency is closely related to the biological affinity pairs, elution conditions and matrix carriers. In principle, the biomarkers (antigens) applied by this method should be high-abundance proteins on the surface of exosome membranes, such as four-transmembrane protein superfamily, ESCRT complex-related proteins. Of course, the target protein can be a common component on the surface of exosomes, or the unique one that promotes IAC to recognize specific cell-derived exosomes. Compared to ultracentrifugation, IAC can produce comparable results with less sample volume. It also can be used for qualitative and quantitative determination of exosomes. It has strong specificity, high sensitivity, high purity and high yield, and does not set the upper limit of the starting sample volume when based on magnetic beads.^16,58,59 For example, the enzyme-linked immunosorbent analysis technique based on microplates is used to enrich exosomes in fluids such as serum, plasma and urine. Quantitative detection and analysis found that the yield of exosomes harvested by this method is equivalent to that of ultracentrifugation, but the demand of samples is much smaller. The amount of RNA extracted from 400 μL plasma is the same as the amount obtained by ultracentrifugation of 2.5mL samples, so there are certain advantages over ultracentrifugation.⁶⁰ Nevertheless, the storage conditions of exosomes obtained by immunoaffinity chromatography are relatively harsh and are not suitable for large-scale separation of exosomes. The non-specific interference adsorption of the matrix will produce interfering proteins, making this method difficult to popularize.

Other Isolation Techniques

There are various commercial kits currently on the market based on the above traditional isolation technology, like exoEasy Maxi kit (QIAGEN), MagCapture™ Exosome Isolation Kit PS (Wako) and Minute™ Hi-Efficiency Exosome Precipitation Reagent (Invent). Comprehensive analysis shows that the commercial kit has the advantages of time saving, high yield, good integrity and so on. However, due to the uneven extraction effect of the current commercial exosome extraction kits, there is still no kit that can isolation the ideal exosomes from the mixture of samples. At the same time, the kit itself is expensive, and the yield and purity of exosomes are not high. But with the continuous exploration, development and innovation of exosome isolation and purification technology, more and more new methods are available for researchers to optimize traditional technologies from one or more perspectives, which has potential application value.

A recent study has developed a new micro-vortex chip, which is integrated with Morpho Menelaus butterfly wings modified with lipid nanoprobes to solve the problem of difficulty in effectively separating and purifying extracellular vesicles from biological fluids. When the body fluid passes through this chip, the generated micro vortices can enhance the interaction force between the extracellular vesicles and butterfly wings, and at the same time, the probe is inserted into the extracellular vesicles to achieve high-throughput enrichment. After testing, it is found that the separation efficiency of this technology exceeds 70% and does not affect downstream analysis, which has potential application value⁶¹. Saliva-derived exosomes are separated and purified based on the size using a newly developed acoustic fluid platform, which combined acoustics with microfluidic technology. The average yield of small RNA in exosomes detected by RT-ddPCR using this technique is 15 times that of differential centrifugation, and studies have found that harvesting exosomes by this technique is beneficial for downstream analysis⁶². In addition, separation techniques such as Tangential Flow Filtration,⁶³ Flow field-flow fractionation (FIFFF)⁶⁴ and Deterministic lateral displacement array⁶⁵ also have good enrichment potential.

Although a variety of methods for the isolation and purification of exosomes have been developed, there are some shortcomings that cannot meet all needs. The combination of different isolation methods may be better than the separation effect of a single method. Therefore, in order to improve the separation efficiency and enrichment, and thus obtain the ideal exosomes, many research teams have begun to combine multiple methods to isolate and purify the exosomes to improve the yield and purity. For example, by combining ultracentrifugation and ultrafiltration to extract exosomes crudely, and then using magnetic beads to adsorb affinity bodies containing colonic epithelial cell-specific A33 antibody by immunoaffinity capture technology to further purify the exosomes. Various exosomal proteins associated with colon cancer have been identified as potential diagnostic biomarkers.⁶⁶ To make up for the deficiencies of the kit based on polymer precipitation method, the research team tried to combine UC with the kit to extract exosomes from human serum. The experiment found that this combination scheme can provide better yield and quality assurance, suitable for further study with large samples to meet the clinical application standard.⁶⁷ Koh et al.⁶⁸ combined UC with SEC, which could not only handle large-volume of samples, but also effectively eliminate the interference of contaminants, so as to draw on each other’s merits. This not only reduced the separation time, but also increased the yield, which was suitable for enriching exosomes from biofluids.

Characterization

The exosome characterization is specific and identical, so several characterization indexes are needed to determine whether the extracted components are exosomes. International Society for Extracellular Vesicles (ISEV) proposed¹⁰ that two types of proteins (like Transmembrane or GPI-anchored proteins associated to plasma membrane and/or endosomes, Cytosolic proteins recovered in EVs) need to be evaluated to determine whether the extracted components are exosomes and exosomes derived from biological fluids can be assessed for their purity by determining the presence or absence of certain non-EV structural protein components co-separated with EV. In general research, we consider the identification of isolated exosomes from three levels, including TEM identification of exosome morphology, NTA identification of exosome size and Western Blot identification of exosome surface protein markers. Exosome characterization methods are mainly divided into two types: external characterization (mainly morphology and particle size detection) and inclusion characterization (like membrane protein, lipid raft). The purpose, advantages and disadvantages of commonly applied methods are shown in Table 1.

Table 1.

Purpose, Advantages and Disadvantages of Common Exosome Characterization Methods

Methods	Purpose	Advantages	Disadvantages
Electron microscope (Scanning electron microscope SEM or Transmission electron microscope TEM)	Detection of exosomal morphology	Electron microscope can directly observe the morphological structure of exosomes, among which SEM can observe the surface structure, TEM can observe the internal structure and provide the information of particle size distribution.69	Due to the complicated operation of TEM and higher requirements on sample preparation than SEM, it is not suitable for rapid measurement of a large number of samples.70 SEM’s resolution is lower than TEM.
Dynamic light scattering technology	Detecting the size of exosomes	The lower limit of measurement is 10 nm, which is suitable for the determination of monodisperse systems.	It is not suitable for measuring complex exosome samples with large size range, the concentration of exosomes cannot be detected, and it is difficult to distinguish contaminated proteins from exosomes.
Nanoparticle Tracking Analysis Technology (NTA)	Detecting the size and concentration of exosomes	The detection speed is fast and the exosomes can be observed in real time. The resolution is higher than the flow cytometer, and the lower limit of the measurement of fluorescent particles can reach 30–40nm.	The operation is complicated and it is difficult to distinguish contaminated proteins from exosomes. Camera levels and detection thresholds will affect the quantification of exosomes.71
Western Blot (WB)	Detection of the expression of exosomal marker proteins	As one of the classic methods, this technique is mature and can qualitatively and quantitatively analyze marker proteins. It is also easier to analyze exosomes from cell culture media.	The operation is complicated and time-consuming. The detection of marker proteins varies depending on the type of parental cell, and it is not suitable for the detection of exosomal marker proteins in biological fluids.10
Enzyme-linked immunosorbent analysis (ELISA)	Detection of the expression of exosomal marker proteins	It has strong specificity and rapid detection, can qualitatively and quantitatively analyze marker proteins, and is suitable for high-throughput analysis.72	The operation is complicated and time-consuming. The repeatability is not good and there are many interference factors.
Flow Cytometry	Detection of biomarkers of exosomes	This method is capable of high-throughput, multi-channel analysis, and the analysis speed is fast, and the required sample concentration is low.	This technique is time-consuming and laborious. The detection limit is 400nm, and the particle size of exosomes cannot be measured. In addition, due to the detection of optical signals, the accuracy and resolution are relatively low, and the characteristics of polydispersity and low refraction limit its application.73

Recently, some characterization methods developed and optimized at home and abroad are available for reference. For example, Islam et al.⁷⁴ provided a way to measure EVs without extensive pretreatment. The NP-TRFIA technology uses biotinylated antibodies that specifically target four transmembrane proteins and tumor-associated antigens to capture EVs from urine and cell supernatants directly, and then the performances of two lanthanide-based tracers are compared for detection and characterization. The signal-to-noise ratio of this method is 2–10 times that of the lectin-chelate assay. Compared with Western blot and flow cytometry, it simplifies the separation step and saves time. At the same time, it can be used to identify and evaluate tumor-associated proteins on the surface of EVs, and has potential for disease diagnosis and prognosis. In addition to marker proteins, specific types of phospholipids present in the lipid bilayer may also be a potential positive control for characterizing the presence of exosomes,^75,76 so it may be considered to develop multiple markers to characterize exosomes in many ways.

Storage Stability

Exosomes are a promising cell-free therapy, but they cannot be stored for a long time. Therefore, it is necessary to study exosomes preservation technology to protect their biological activities and make them convenient for transportation and clinical application. Currently, the applied protection techniques mainly include freezing, freeze-drying and spray-drying.

Cryopreservation

Cryopreservation is a storage method that reduces the temperature below the temperature required for biochemical reactions to maintain the functional stability of the biological particles, and is usually applied at the temperature of 4 °C, −80 °C and −196 °C. However, this storage method is prone to “frostbite”. The “frostbite” described here is mostly related to the imbalance of osmosis during the freezing process and the formation of ice crystals inside the biological particles. In order to overcome this deficiency, one or more antifreezes with appropriate concentrations are often added selectively to extend the shelf life.^77–79

Antifreeze is usually divided into two types of permeability and non-permeability. Among them, the permeable antifreeze has a small molecular weight and can penetrate the cell membrane into the cell to prevent the formation of ice crystals, such as dimethyl sulfoxide and ethylene glycol. Studies have shown that from a morphological perspective, direct freezing affects the stability of exosomal membranes and promotes their degradation, while DMSO-added exosomes in cryopreservation are similar to fresh exosomes. Moreover, in terms of biological activity, Short-term cryopreservation (within 2 months) did not significantly change the function of exosomes.⁷⁰ Non-permeable antifreeze can form hydrogen bonds with water, usually trehalose, sucrose and other carbohydrates. Sugar replaces the water molecules around the lipid head group through the interaction between the phospholipid head group and the OH part of the sugar. The glass matrix of the sugar can prevent the aggregation of vesicles and reduce the damage caused by ice crystals.⁸⁰ Considering the safety, the disaccharide antifreeze is the best choice for exosomes, among which trehalose is listed as the most effective disaccharide antifreeze.⁸¹ It is worth noting that the appropriate concentration of antifreeze should be examined before use to maintain a balanced state and prevent unnecessary injury.

Freeze-Drying

Freeze-drying is a technology that cools materials containing moisture in advance and freezes to a solid below freezing point, directly sublimates the ice under vacuum and removes it in the form of water vapor, thus meeting the storage requirements. Freeze-drying technology is mainly divided into three stages: pre-freezing stage, sublimation drying stage and analytical drying stage. The freeze-dried exosomal lyophilized powder can effectively reduce the storage conditions. Because it completes the dehydration and drying of products under low temperature and vacuum conditions, it can maintain its original activity and reduce the damage to biological tissues and cell bodies. The material can be easily kept in a constant storable state, and can be reconstituted by simply adding water. It is a suitable method for preserving heat-sensitive materials such as EVs, vaccines, and proteins.

During the freeze-drying process, the molecular structure of the biomolecule may be destroyed due to the freezing and dehydration pressures generated. Therefore, it is also necessary to selectively add antifreezes to protect the biological material. Charoenviriyakul et al.⁸² divided the exosomes from B16BL6 melanoma into three parts, one of which was stored at −80°C, one of which was freeze-dried with trehalose added, and one of which was freeze-dried directly, and compared the morphology, protein content and the influence on pharmacokinetics of the exosomes. The results show that the addition of trehalose can effectively prevent the aggregation of exosomes during the freeze-drying process, increase its colloidal stability, and do not change the morphology of exosomes. The protein content of lyophilized exosomes stored at room temperature was similar to that at −80°C, and the effect on pharmacokinetics was minimal.

Spray-Drying

Spray drying is a technique applied systematically to the drying of materials. After the EVs solution is atomized in the drying room, the moisture quickly vaporizes in contact with the hot air to obtain dry powders. During the process, the atomization pressure and outlet temperature are factors that affect the stability of exosomes. Compared with lyophilization, spray drying is a continuous process, which can realize one-step milling, which is more economical, and is expandable and can adjust the particle size of products.⁷⁹

To date, the best comprehensive storage way is −80 °C frozen storage. However, different sources and different experimental techniques all affect the temperature selection of long-term storage stability of exosomes. Studies have found that compared with freshly extracted exosomes, storage at −80 °C for 4 days will change the morphology of exosomes,⁸³ and the biological activity of exosomes will be reduced during storage at −80 °C for 28 days.⁸⁴ At the same time, some studies have shown that milk-derived exosomes are stored at −80 °C for four weeks without any change in physical properties, and the loading rate of paclitaxel also remains stable.³⁵ Therefore, it is urgent to study the storage stability of exosomes from multiple perspectives, especially the long-term stability. For example, from the perspective of source, drug delivery route, application technology and future research direction. In short, it is beneficial to carry out subsequent functional studies of exosomes, shorten the experimental process and expand their application scope.

Applications

Disease Diagnosis

Exosomes are rich in biomarkers for disease diagnosis and prognosis. They are mainly applied in cancer and have also made some progress in the fields of cardiovascular diseases, tuberculosis and central nervous system diseases. The level of exosomal microRNAs associated with cardiovascular diseases including miR-499, miR-133, miR-208, miR-192, miR-194, miRNA-34a is up-regulated in patients with acute myocardial infarction and heart failure,^85–88 which provides a strong basis for their use as a diagnostic marker. It is reported that Dysferlinopathy is a kind of disease caused by the lack of dysferlin. Yin’s team⁸⁹ evaluated the diagnostic ability of exosomes in the serum and urine of patients with this disease, and found that there is no dysferlin in exosomes from patients, which can be distinguished from normal people for the diagnosis of Dysferlinopathy. MiR-21, miR-29, miR-219, LRP6, REST1, caveolin1 in exosomes are differentially expressed in central nervous system diseases, showing good clinical diagnostic potential.^90–93

Liquid biopsy is a minimally invasive, convenient and fast diagnostic method in vitro for tumor sampling. Tumor exosomes can promote tumor formation in the process of normal cell carcinogenesis. They are highly enriched in biofluids and can be used for liquid biopsy. Because the expression of biologically active substances carried by exosomes in healthy people and tumor patients is different, the detection of biomarkers that predict cancer in tumor exosomes can help improve the specificity and sensitivity of early diagnosis of tumors. For example, exosomal protein CD151 is highly expressed in patients with lung cancer,⁹⁴ miR-1246 and miR-21 are highly enriched in exosomes derived from breast cancer cells,⁹⁵ and miR-638 can be used as a diagnostic marker for colorectal cancer.⁹⁶ Exosomal miRNA is the most commonly used biomarker with tissue specificity. Studies have found that exosomes are rich in miRNA, and the membrane structure of exosomes can enhance the stability of miRNA molecules and enhance their potential as disease biomarkers. In 2016, Exosome Diagnostics launched the world’s first cancer diagnostic product-ExoDX Lung (ALK). The product is based on exosomal detection technology, which can simultaneously detect exosomal RNA and ctDNA, and perform real-time screening for EML4-ALK mutations in patients with non-small cell lung cancer. According to data provided by Exosome Diagnostics, ExoDx Lung (ALK) has a sensitivity of 88% and a specificity of 100% in detecting non-small cell lung cancer, which can be used to assist doctors in determining whether patients are suitable for ALK inhibitor targeted therapy, especially for those patients who are unable or unwilling to undergo tissue biopsy.

Disease Treatment Through Exosome-Targeted Drug Delivery System

Exosomes are small in size, which can effectively avoid the phagocytosis of mononuclear macrophages, and can freely cross the blood vessel wall and extracellular matrix. The expression of CD55 and CD59 on its surface avoids the activation of opsonin and coagulation factors, so it can be widely distributed and stable in the biofluids. Compared to liposomes and other nano-delivery systems which are synthesized in vitro, exosomes originate from the body, and have better biocompatibility and lower immunogenicity in theory. In fact, due to the heterogeneity of exosomes, they carry various proteins on the surface, which enter the cells in a variety of ways after contacting with cells. Among them, receptor-mediated endocytosis is one of the main ways of information communication between exosomes and target tissues, which optimizes the endocytosis process of exosomes and promotes the internalization of the encapsulated drug and facilitates the continuous and stable transport of the contents in the blood with high transport efficiency. Moreover, exosomes have strong ability to homing target tissues or cells and penetrate biological barriers (like the blood-brain barrier), so they have the advantage of natural drug delivery and are promising targeted drug carriers, which can be used to deliver genetic drugs, traditional Chinese medicine, western medicine, and so on.^97,98 However, natural exosomes may have problems such as weak targeting and susceptible to be quickly cleared in the body, resulting in poor treatment effect. At this time, they are usually modified to form engineered exosomes. Engineered exosomes refer to natural exosomes loaded with therapeutic agents or modified. In the following part, the applications of targeted delivery system of exosomes will be explained mainly from the perspectives of drug loading and surface modification.

Type of Drug Loading

Western medicine is one of the therapeutic agents delivered by exosomes as drug carriers, which can play a role in various pathological processes such as cancer and inflammation. The mortality rate of cancer has been high for a long time, and it is the goal of research teams at home and abroad to develop efficient cancer treatment strategies. Doxorubicin is an amphiphilic drug, which can inhibit angiogenesis and control tumor growth to play a therapeutic role. It belongs to a broad-spectrum antitumor drug. Yang et al.⁹⁹ used the zebrafish model to examine the efficacy of brain endothelial-derived exosomes to deliver the anti-tumor drug doxorubicin through the blood-brain barrier. The image shows that exosomes successfully loaded the drug across the blood-brain barrier, which can significantly inhibit the growth of tumors, confirming that exosomes can act as a carrier. In addition, anti-cancer drugs such as porphyrin,¹⁰⁰ tirapazamine,¹⁰¹ docetaxel and cisplatin can also exert their effects through exosomes.

Catalase (CAT) is one of the most effective antioxidants. It can inhibit inflammation and protect dopaminergic neurons. It can be used to treat neurodegenerative diseases. Neurodegenerative diseases are caused by the loss of neurons and/or their myelin sheaths and are generally diagnosed based on clinical symptoms. The presence of the blood-brain barrier (BBB) limits the application of nearly 98% of central nervous system disease treatment agents, and clinical application is extremely difficult.¹⁰² Chronic diseases require long-term drug treatment^103,104. When investigating the therapeutic effect of CAT on Parkinson’s disease, Haney et al.¹⁰⁵ found that encapsulation of CAT with exosomes can effectively reduce oxidative stress and increase the survival rate of neurons in both in vivo and in vitro models of PD. At the same time, loading CAT on exosomes can maintain its biological activity, reduce immunogenicity, prolong blood circulation time, and solve its deficiencies of easy inactivation and rapid degradation, thereby enhancing the therapeutic effect. In summary, Exo-CAT preparation is expected to become a general strategy for the treatment of neurodegenerative diseases.

Traditional Chinese medicines, including monomeric active ingredients and compound preparations, have been widely used in the study of exosome delivery systems due to its low toxicity and side effects.

Although paclitaxel (PTX) is a widely used antitumor drug, which can play a therapeutic role in a variety of malignant tumors,³⁵ it is a highly hydrophobic compound and has dose-dependent toxic and side effects, so its clinical application is limited.^106,107 Recently, studies using exosomal delivery of PTX to address this deficiency have been widely reported. For example, Wang et al.¹⁰⁸ selected classical activated M1-type macrophage-derived exosomes as a carrier to reduce the toxicity of PTX and improve its bioavailability. Not only has PTX been successfully delivered to tumor tissue of mice, but also by activating NF-κB pathway it establishes a pro-inflammatory environment to enhance the therapeutic effect of PTX.

Curcumin is a lipophilic polyphenolic compound. Its low solubility, poor stability, fast metabolism, short half-life and other defects lead to lower bioavailability, which limits its application in the treatment of diseases. Sun et al.¹⁰⁹ loaded curcumin onto exosomes to form a complex that enhanced its anti-inflammatory activity by improving the solubility, stability and bioavailability of curcumin. Mice treated with this complex were able to resist lipopolysaccharide (LPS)-induced septic shock. In addition, curcumin also has anti-tumor, anti-oxidation, anti-atherosclerosis and other effects.

Exosomes loaded with berry anthocyanins have good inhibitory activity against the proliferation of ovarian cancer cells.¹¹⁰ Exosomes carrying catalpol can play a neuroprotective role.¹¹¹ β-elemene-loaded exosomes can inhibit the proliferation and migration of tumor cells and also have a certain improvement in drug resistance to cancer cells.^112,113 In addition, exosomes can also be loaded with triptolide¹¹⁴ or the traditional Chinese medicine compound Buyanghuanwu Decoction¹¹⁵ to make up for the lack of single administration and enhance the therapeutic effect.

Exosomes can also deliver gene therapeutic agents such as DNA and RNA and adopt gene therapy strategies. For example, oligonucleotides can silence specific genes to treat a variety of human diseases, including cancer or neurodegenerative diseases. Oligonucleotide agent (ONT) is a kind of new drugs that prevents the expression of proteins that cause disease phenotypes by targeting RNA or DNA, such as delivering exosomes loaded with hydrophobic siRNAs (hsiRNAs) which target Huntingtin mRNA to the brain is an effective treatment for Huntington’s disease and other neurodegenerative diseases¹¹⁶. Similarly, exosomes can carry therapeutic RNA to target cells, such as targeting exogenous siRNA to monocytes and lymphocytes in human blood cells, which can cause MAPK1 gene to silence selectively.¹¹⁷

Route of Administration

The exosome delivery system has various routes of administration, among which the common routes include intravenous injection,^118,119 subcutaneous injection,¹²⁰ intraperitoneal injection,^121,122 intratumoral injection,¹²³ nasal administration^{32,105,124,125} and oral administration.³⁵ Essentially, the route of drug administration is closely related to the therapeutic effect of various diseases, and different routes of drug administration also affect the biological distribution and rapid clearance rate of drugs in vivo. Therefore, it is necessary to investigate the influence of the routes of exosome drug delivery system.

Drug Loading Ways

According to whether the therapeutic agent is directly loaded on the exosomes, it is mainly divided into two major drug loading types: pre-secretory drug loading and post-secretory drug loading. Pre-secretory drug loading means that the therapeutic agent originates from or is loaded on the parent cell to secrete engineered exosomes. This type of operation is simple, but the drug loading efficiency cannot be controlled, and the natural physiological function of membrane proteins may be damaged. As the name implies, post-secretory drug loading refers to the direct addition of therapeutic agents to exosomes in a certain way, but exosome aggregation, membrane damage and low yield may exist^101,126,127. Electroporation and ultrasonic treatment are the most commonly used methods of drug loading because of their relative convenience and efficiency. The drug loading rate of exosomes may be related to the hydrophobicity of drugs, the drug loading method, the lipid composition of exosomes, etc.¹⁰⁰. Therefore, in the actual study, the appropriate drug loading method is mainly selected according to the physical or chemical characteristics of the drugs and the common method is shown in Figure 2.

Figure 2.

Common drug loading ways of exosomes.

The method of gene editing uses genetically modified parent cells as the main strategy to integrate the therapeutic agent into the corresponding exosomes, and is suitable for RNA or proteins that cannot be directly loaded onto exosomes. Sterzenbach et al.¹²⁴ used the L-domain-containing protein Ndfp1 to recognize the WW-tagged target protein Cre recombinase, thereby loading the target protein into exosomes during MVB formation. Flow cytometry showed that the WW tag did not affect Cre recombinase activity. Such exosomes can cross the blood-brain barrier to deliver bioactive proteins, providing a new strategy for the treatment of brain diseases. In another study, FAM miR-125a was used to transfect human adipose-derived MSCs, and miR-125a overexpressed exosomes were obtained. It was found that miR-125a in exosomes plays a key role in endothelial cell angiogenesis¹²⁸. There are also commercial transfection reagents on the market, like HiPerFect transfection reagent and Lipofectamine 2000, to load siRNA directly into exosomes. However, it is clear that this method is relatively inefficient in loading and relatively complicated to operate. Therefore, Li et al.¹²⁹ constructed a CD9-HuR fusion protein, in which HuR is an RNA-binding protein located inside the exosomes, and selectively enriched the target miR-155 into the exosomes. This method does not destroy RNA structure, has a strong ability to enrich specific RNAs, significantly improves loading efficiency, and is expected to become a new strategy for clinical trials of gene delivery in vivo.

There are two forms of co-incubation. One is to co-incubate the therapeutic agent with parental cells to disperse the therapeutic agent or to load part of the therapeutic agent in the cytoplasm into the secreted exosomes by means of endocytosis by parental cells. The other is that exosomes and therapeutic agents are directly co-incubated and mixed under appropriate conditions. Their loading efficiency mainly depends on the concentration gradient of the drug in the solution and its hydrophobicity. The hydrophobic drugs with high concentration usually have relatively high loading efficiency.¹⁰⁵ The method is easy to operate, highly reproducible, and does not affect the integrity of exosome membrane structure, but the loading efficiency is low, and a large number of therapeutic agents are needed. It is also necessary to investigate whether the therapeutic agents have toxic side effects on parental cells and affect the stability by changing the surface charge of exosomes.

Electroporation is to expose the suspension of exosomes and therapeutic agents to the electric field. The exosome membranes will produce temporary pores under a short high-voltage pulse, so the therapeutic agents will penetrate into the exosomes. Electroporation is a relatively mature method, which is simple and time-saving, and can be used to load nucleotides, doxorubicin and other drugs into exosomes¹³⁰. The exosomal concentration will affect the efficiency of electroporation. Wahlgren et al.¹¹⁷ used exosomes from peripheral blood as carriers to deliver therapeutic siRNA by electroporation. In the experiment, the effects of exosomal concentration, siRNA concentration and electroporation parameters on the efficiency of electroporation were investigated. It was found that changes in siRNA and capacitance did not affect the electroporation efficiency, and the electroporation efficiency was the highest when the exosome concentration was within the range of 0.25–1 mg/mL. However, this method also has disadvantages, such as destroying the integrity of the membrane structure, reducing the loading efficiency and low loading rate. The use of high-voltage pulses will cause exosomes to aggregate. At the same time, this method may destroy the protein structure and affect its activity, which limits its application.

Sonication is highly efficient in drug loading and can sustainably release drugs, especially hydrophobic drugs, and can prevent protease destruction. However, this method may lead to aggregation of exosomes and affect their immune activity, which not only requires high requirements on the instrument, but also may damage the plasma membrane structure of exosomes and cause drug leakage, resulting in unsatisfactory drug loading. Sonication may alter the high rigidity of the membrane, and recombination of exosomal membranes results in high loading efficiency and sustained drug release. Kim et al.³² compared the loading rates of the three loading methods of co-incubation, electroporation and sonication, and the results showed that the load capacity of exosomes treated by sonication was the highest, confirming the above hypothesis. Similarly, Salarpour et al.¹³¹ investigated the effects of 37 ° C co-incubation and sonication on the encapsulation efficiency of PTX (hydrophobic drugs), and found that the loading of sonication (9.21 ± 0.41 ng/μg) was higher than that of co-incubation (7.40 ± 0.37 ng/μg), which gave similar results to Kim.

Extrusion usually uses an extruder to achieve drug loading of exosomes. During the extrusion process, the exosomal membrane is broken and violently mixed with therapeutic agents.¹³² The method of extrusion can obtain higher drug loading. For example, compared with co-incubation and freeze-thaw cycles, exosomes loaded with catalase (CAT) by extrusion have the highest encapsulation rate and show strong catalytic activity. Therefore, such exosomes provide the most effective neuroprotective effect, which is due to the remodeling of exosomal membranes by extrusion so that CAT diffuses through the relatively tight and highly structured lipid bilayer, thus resulting in a high encapsulation rate.¹⁰⁵ However, it may damage the plasma membrane structure of exosomes and cause drug leakage. Whether cytotoxicity will be produced remains to be studied.

The freeze-thaw cycle is a physical and chemical process that simply mixes exosomes with drugs and freezes at −80 ° C or liquid nitrogen, and then thaws at room temperature.^132,133 The drug loading capacity of the freeze-thaw cycle is usually lower than that of sonication and extrusion. Exosomes may aggregate and cause an increase in size. In addition, proteins are also easily degraded to affect biological activity.

In the process of the Saponin-assisted treatment, saponin is an effective permeabilizing agent for the cytoplasmic membrane. It selectively forms a complex with cholesterol bound to exosomal membranes to form a porous structure on the membrane surface, which promotes the incorporation of therapeutic agents. Studies have found that saponin-treated exosomes loaded with ProBA [meso-Tetra(4-carboxyphenyl) porphine] have a high drug loading rate, and the drug intake is about 8%, which is significantly higher than that of free drugs (2%), so it can be shown that saponin-assisted treatment enhances the loading of porphyrins in exosomes without affecting the drug delivery capacity.¹⁰⁰ However, saponins are a class of surfactants that are hemolytic in vivo, so the concentration of saponins needs to be limited, and exosomes should be washed and purified immediately after co-incubation.^132,134

In summary, the above methods do not allow the combination of therapeutic agents with different properties to be loaded simultaneously, whether the pre-secretory loading or the post-secretory loading. Lee et al.¹⁰¹ applied liposomes to the surface modification of extracellular vesicles. MFL (membrane-fused liposomes) can effectively co-load a lipophilic drug (Paclitaxel) and a hydrophilic drug (Tirapazamine) into extracellular vesicles simultaneously, without affecting the original functional expression of membrane proteins. Thus, it can be considered as a general strategy. In short, no matter which method is adopted in practical application, factors such as drug properties, drug loading, efficiency, damage to exosome membranes, and influence on subsequent experiments should be considered comprehensively to find the best method.

Surface Modification

Surface modification is the process of treating exosomal surface proteins as anchoring devices or affinity tags, and modifying the protein or peptide components that meet the requirements to the particle surface by certain means. Natural exosomes need to be superficially modified if they are unable to effectively deliver drugs or targeted applications due to their inadequacy, such as poor stability and rapid elimination.²⁹ One of the biggest advantages of exosomes is endogenous, which can avoid causing adverse manifestations such as immune response. However, the efficiency of exosomal delivery is affected by parental cells and receptor cells. The yield of exosomes from different sources is significantly different, and natural exosomes have the problem with poor-targeting. In order to meet the experimental needs, surface modification to manufacture engineered exosomes is a way of practical application value. Surface functionalization of exosomes with targeted ligands can help them be selectively delivered to target cells and enable exosomes to reach standards in terms of yield and targeted therapy, so as to achieve precise treatment of exosomes and accelerate the clinical application of exosomes.

In order to precisely target therapeutic drugs to the lesion, the methods commonly used in recent years include chemical linking of targeting peptides, modification of exosomal membranes or progenitor cells by genetic engineering, magnetic nanoparticle technology, electrostatic interaction and post-insertion. Applications of partial surface modification exosomes are listed in Table 2.

Table 2.

Application Examples of Surface Modification

Surface Modification Methods	Targeting Method	Drug Loading	Targeted Tissues and Applications	Ref.
Genetic Engineering	Dendritic cells (DCs) are genetically modified to express fusion proteins containing the membrane protein Lamp2b and RVG peptides, and engineered exosomes are harvested from the cells.	siRNA (Electroporation)	Targeting the central nervous system (neurons, microglia, oligodendrocytes) to treat Alzheimer’s disease	[126]
Chemical reaction combined with post-insertion	c (RGDyK) is a tumor-targeting peptide. DSPE-PEG 2000-cRGDyK is prepared by chemical reaction. The ligand is spontaneously inserted into the exosomal lipid bilayer through hydrophobic interactions and combined to obtain the targeted exosomes.	PTX (Co-incubation)	It can penetrate the blood-brain barrier, target glioblastomas, and significantly reduce the activity of cancer cells.	[135]
Genetic Engineering	Donor cells are engineered to express the transmembrane domain of the platelet-derived growth factor receptor fused to the GE11 peptide to achieve targeting, thereby assimilating exosomes from this source.	let-7a miRNA (Transfection)	Targeting breast cancer tissues expressing EGFR to treat breast cancer	[136]
Genetic Engineering	Engineered mouse immature dendritic cells expressing Lamp2b fused to iRGD peptide to produce tumor-targeted exosomes.	DOX (Electroporation)	It targets tumor tissues, inhibits the growth of tumor, and has good antitumor activity.	[119]
Chemical reaction	Extracellular vesicles containing azide lipids were firstly prepared and then conjugated to the targeted peptide using a copper-free catalytic click chemistry.	PTX, TPZ (Loaded on liposomes)	Targeting tumor cells	[101]
Electrostatic interaction	The complex formed by a cationic lipid and a pH-sensitive fusion peptide binds exosomes through electrostatic interaction to target the receptor cell membrane.	Dextran, Saponin (Electroporation)	Targeting the receptor’s cell membrane to enhance cell uptake and cytoplasmic release of exosomes	[137]
Magnetic nanoparticle technology	The SPMN-Tf conjugates were co-incubated with pre-dialyzed serum to form SMNC-Exo through interaction with the Tf-Tf receptor. After drug loading, SMNC-Exos were concentrated in the tumor region in the presence of an external magnetic field.	DOX (Co-incubation)	Targeting mouse subcutaneous H22 cells to inhibit the growth of tumor	[138]

There is no doubt that surface-modified exosomes have certain advantages, but engineering exosomes also have certain limitations. First, surface modification of exosomes cannot change the structure and surface molecules of exosomes, while chemically linked targeting peptides have the potential to alter the surface structure of exosomes. Furthermore, the operation of genetically modified parental cells is complex, and the transfection efficiency is low, which is easy to affect the original biological activity of membrane proteins. When exosomes are modified with virus-derived proteins (or peptides), it is necessary to evaluate whether there is an adverse reaction to themselves. In addition, cationic nanomaterials used in electrostatic interactions may cause cytotoxicity and the loading efficiency is relatively low.

Based on the limitations of the popular surface modification methods currently, professor Yin’s team screened out the phage CP05 coupled targeting molecules (M12, RVG, SP94) to form a chimeric peptide, and then combined them with CD63 on the exosomal surface to capture exosomes from different sources. The method has a high modification efficiency. Not only is the amount of exosomes caught large, but also the targeting can be enhanced, so that the modified exosomes can be enriched respectively in muscle, brain and subcutaneous tumors. CP05-modified exosomes have not changed significantly in their physiological characteristics, have not changed the structure and surface molecules of exosomes, and are expected to be used for rapid detection of clinical cancer and effective carriers for therapeutic drugs.¹³⁹ In addition, Tamura et al.¹⁴⁰ used cationized amylopectin to modify the exosomes to make them have the ability to target the asialoglycoprotein receptor of hepatocytes, which helps to achieve precise treatment of exosomes and enhance treatment effect. Lee et al.¹⁰¹ also optimized the method of chemically linking and targeting peptides. The parent cells were treated with azide-MFL to generate azide-EVs, which were then linked with the tumor-targeting peptide conjugate DBCO-CGKPK through a biological orthogonal reaction. In this process, DBCO- CGKPK uses copper-free catalytic click chemistry to connect. Such engineered EVs can be used to load therapeutic agents internally and externally can be modified with multiple functions. Exogenous incorporation of MFL for surface modification does not affect membrane proteins that play a decisive role in the biological function of EVs.

Engineered exosomes do not have absolute advantages in drug delivery applications. Some studies have found that the same loading method is used to load cholesterol-modified siRNA to prepare engineered exosomes and anionic fusion liposomes respectively to compare their delivery capabilities. Engineered exosomes cannot functionally deliver relevant small RNAs, while anionic fusion liposomes can induce siRNA-mediated knockout of target genes.¹⁴¹ Therefore, when considering whether to apply engineered exosomes, it is necessary to combine with the actual situation and have a deep understanding of the molecular transfer mechanism and specificity, and blind application should be avoided by all means.

Conclusions

Compared with liposomes, nanoparticles, microspheres, microemulsions and other synthetic drug loading systems, the endogeneity of exosomes is a natural and unique advantage. The superiority of exosomes makes it an important medium for cell-to-cell communication, and it plays unique biological functions in regulating the normal life activities and in the diagnosis and treatment of diseases. Exosomes, as current research hotspots, have received extensive attention from researchers at home and abroad. However, the detection technologies for the diagnosis and prognosis of diseases using exosomal contents as markers have not been perfected. Whether exosomes can be used clinically as soon as possible depends largely on the results of optimization and improvement of the existing exosome problems. How to improve the yield and purity of exosomes is the top priority, which has always been the bottleneck limiting its transformation application. Studies in recent years have shown that the appropriate combination of several methods to extract and purify exosomes can effectively improve the above problems, and how to combine them to achieve the best results remains to be further studied. Secondly, the secretion mechanism and fusion mechanism of exosomes are still unclear. The impact of exosome heterogeneity on drug loading efficiency needs to be further revealed. Exosome loading capacity and methods for enhancing targeting also need to be optimized and improved. Carry out all-round and multi-field researches to analyze its biological functions and lay the foundation for subsequent pharmacokinetics, toxicology research, and clinical testing, which will help to better understand the state of the body and diagnose and treat diseases in the future.

Funding Statement

This work was supported by the National Natural Science Foundation of China (81803738).

Disclosure

The authors have declared that there is no conflict of interest.