Intraperitoneal Route of Drug Administration: Should it Be Used in Experimental Animal Studies?

Abstract

Intraperitoneal (IP) route of drug administration in laboratory animals is a common practice in many in vivo studies of disease models. While this route is an easy to master, quick, suitable for chronic treatments and with low impact of stress on laboratory rodents, there is a common concern that it may not be an acceptable route for drug administration in experimental studies. The latter is likely due to sparsity of information regarding pharmacokinetics of pharmacological agents and the mechanisms through which agents get systemic exposure after IP administration. In this review, we summarize the main mechanisms involved in bioavailability of IP administered drugs and provide examples of pharmacokinetic profiles for small and large molecules in comparison to other routes of administration. We conclude with a notion that IP administration of drugs in experimental studies involving rodents is a justifiable route for pharmacological and proof-of-concept studies where the goal is to evaluate the effect(s) of target engagement rather than properties of a drug formulation and/or its pharmacokinetics for clinical translation.

INTRODUCTION

It is well-recognized that the route of administration is a critical determinant of the final pharmacokinetics, pharmacodynamics as well as toxicity of pharmacological agents (1). Intravenous (IV), subcutaneous (SC), intraperitoneal (IP) and oral routes are the main paths of drug administration in laboratory animals, with each offering advantages and disadvantages depending on specific goal(s) of the study. One of the more commonly used routes in rodent studies is the IP route where a pharmacological agent is injected into peritoneal cavity. This easy to master technique is quick and minimally stressful for animals. It involves holding of the rodent in a supine position with its head tilted lower than the posterior part of the body and insertion of the needle in the lower quadrant of the abdomen (at ~10° angle) with care to avoid accidental penetration of the viscera (2–4). Large volumes of solution (up to 10 ml/kg) can be safely administered to rodents through this route (5) which may be advantageous for agents with poor solubility. This route is especially common in chronic studies involving mice for which repetitive IV access is challenging. In most cases, IP administration is also preferred over the oral route for biological agents to avoid the GI tract and potential degradation/modification of biopharmaceuticals. The main disadvantage of this route is that it is minimally used in clinic (mostly for treatment of peritoneal cancers), because of which its use in experimental studies is often questioned and discouraged. To mitigate this concern, in this review article we discuss the anatomy and physiology of the peritoneal cavity, and the mechanisms governing absorption of substances from peritoneal cavity. In addition, we provide examples and compare pharmacokinetic profiles of small and large molecules upon IP and other routes of administration in experimental animals. Based on the discussed experimental evidence, we conclude that IP administration of drugs in experimental animals is a justifiable route for pharmacological and proof-of-concept studies where the goal is to evaluate the effect(s) of target engagement rather than properties of a drug formulation and/or its pharmacokinetics for clinical translation.

ANATOMY AND PHYSIOLOGY OF PERITONEAL CAVITY

Peritoneal cavity is a closed space within the abdomen that contains the abdominal organs and is derived from the coelomic cavity of the embryo. Peritoneal cavity is lined by the most extensive serous membrane in the body (i.e., peritoneum) which has total surface area equaling to that of the skin surface (6). Peritoneal cavity is filled with a thin film of fluid (peritoneal fluid) comprised of water, electrolytes, proteins, cells and other substances originating from the interstitial fluid of the adjacent tissues. In humans, the volume of peritoneal fluid ranges from 50 to 75 ml (7), whereas in mice its volume ranges between 0.02 and 0.1 ml (8). In addition, the peritoneal fluid contains leukocytes and antibodies to fight off infections, and plasma proteins at concentration that is about 50% of what is found in plasma (9).

Peritoneum covers most of the intra-abdomenal organs and consists of a single layer of squamous mesothelial cells (10). The mesothelial cell layer sits on a thin basement membrane and the majority of these mesothelial cells are flattered type with an approximate diameter of 25 μm. Mesothelial cells are closely connected to each other by either tight junctions, adherens junctions, gap junctions or desmosomes (11). The sub-mesothelial layer of peritoneum contains collagen, adipose tissue, lymphocytes, blood vessels as well as lymphatics (12). Fibroblasts and occasional macrophages are also present in this part of the peritoneum (13). Notably, the apical surface of mesothelial cells contain microvilli of different length, shape and density, which increase the functional surface area of the peritoneum (Fig. 1) (14).

Fig. 1.

Panel (a), parietal mesothelial cell with small number of pinocytic vesicles and a more mature basement membrane. Panel (b), visceral mesothelial cell with higher number of pinocytic vesicles and less mature basement membrane.

Peritoneal mesothelial cells play crucial role in maintenance of peritoneal homeostasis and transport of fluids and solutes across the membrane. Intra-abdominal organs and mesentery are supported by the visceral peritoneum, whereas the parietal peritoneum lines up the abdominal wall, pelvis, anterior surfaces of retroperitoneal organs, and inferior surface of the diaphragm. The peritoneum minimizes friction and facilitates free movement between abdominal viscera, resists or localizes infection, and stores fat, especially in the greater omentum (15,16). Importantly, the peritoneal mesothelial cells possess many features of epithelial cells including presence of polygonal, cobblestone morphology with surface microvilli and an ability to form a polarized monolayer that permits unidirectional transport of molecules (17). The peritoneal fluid has a pH of 7.5–8.0 and buffering capacity (18), because of which substances are rarely ionized in the peritoneal cavity after IP administration (19).

PERITONEAL BLOOD FLOW

The sub-mesothelial layer of the peritoneum supports a complex but efficient vascular network of blood and lymphatic vessels (20,21). Most of the circulatory vessels are blood capillaries but few arterioles and venules are also present in the sub-mesothelium (22). The density of these sub-mesothelial microvessels varies along different portions of the peritoneal cavity. For example, in the rabbit, the most vascularized area of peritoneal cavity is mesentery, which contains about 71% of peritoneal microvessels, whereas the diaphragm and parietal peritoneum contain about 18% and 11% of microvessels, respectively (21,23). Through these capillaries, peritoneal cavity receives 4 to 7% of the total cardiac output in the rabbit (24) and rat (25,26). The average peritoneal blood flow rate in the rat is 2.5–6.2 ml/min/kg (24). Notably, blood supply to visceral peritoneum and intra-peritoneal organs originates from the coeliac, superior and inferior mesenteric arteries, whereas the parietal peritoneum is irrigated form the branches of circumflex, iliac, lumbar, intercostal and epigastric arteries (27,28). Similarly, the venous system that drains from the visceral peritoneum empties into portal vein, whereas the veins that drain from the parietal peritoneum empty into the inferior vena cava (28,29). Overall the entire peritoneum is well perfused with blood capillaries and provides an excellent surface for exchange of drugs between the peritoneal cavity and plasma (24).

PERITONEAL LYMPHATIC SYSTEM

Like many other organs, peritoneum has a well-structured lymphatic network which maintains the solute and fluid balance of peritoneal tissues and prevents formation of edema (30,31). In the sub-mesothelial layer of the peritoneum, the terminal lymphatic capillaries are subdivided into parasternal, paravertebral, mediastinal, intercostal and retroperitoneal lymphatics. Parasternal, mediastinal and retroperitoneal lymphatics are arranged over the anterior, posterior and central part of the diaphragm, respectively. These terminal lymph capillaries unite together to form afferent collecting and prenodal lymphatic ducts which are then connected with regional lymph nodes. The parasternal, paravertebral and mediastinal lymphatics are connected with the mediastinal lymph nodes, whereas, retroperitoneal lymphatics are joined with cisternal and intestinal lymph nodes. From these lymph nodes the lymphatic system joins the venous circulatory system through thoracic duct and right lymphatic duct (32).

ABSORPTION OF SOLUTES FROM THE PERITONEAL CAVITY, GENERAL CONSIDERATIONS

Peritoneal cavity is an excellent portal of entry into systemic circulation for substances after IP administration. Its large surface area, estimated about 125 cm² in an average rat, presence of microvilli on mesothelial cells and the vast blood supply facilitate rapid absorption of substances after IP administration (33,34). Additionally, lymphatic transport of substrates significantly contributes to the total transfer from the peritoneal cavity to systemic circulation (35).

To reach the vascular compartment after IP administration, a compound must cross different structures in and around the peritoneal cavity including the peritoneal fluid, mesothelium, sub-mesothelium and blood vessel wall (36,37). Transcellular and intercellular spaces in the visceral and parietal mesothelium are the main gateways for solutes and molecules to pass from the peritoneal cavity into surrounding tissues. Because of its structural features, visceral mesothelium is more permeable to molecules compared to parietal mesothelium. Anatomically, visceral peritoneum is composed of flat cells with large number of pinocytic vesicles which facilitate absorption of molecules. On the contrary, parietal peritoneum contains less pinocytic vesicles and has a more developed basement membrane/connective tissue which make it less permeable for molecules (Fig. 1) (38).

Experimental studies indicate that small to medium size molecules (MW < 5000) and fluids are predominantly absorbed from visceral peritoneum by diffusion through the splenic, inferior and superior mesenteric capillaries and drain into the portal vein (39). On the other hand, large molecules (MW > 5000), proteins, blood and immune cells are taken up by the lymphatics (Fig. 2) (40). It is noteworthy, that there is some amount of retrograde movement, of both small and large molecules, from capillaries to peritoneal cavity, however it minimally affects the overall absorption of pharmacological agents from peritoneal cavity to systemic circulation (41,42).

Fig. 2.

Schematic overview of absorption pathways for small and macromolecules from the peritoneal cavity to systemic circulation.

The physiological mechanisms of fluid and solute movement from peritoneal cavity-to-blood or blood-to-peritoneal cavity are the same, either through diffusion or convection. Rapid absorption of small molecules from the peritoneal cavity into blood capillaries are mainly governed by effective surface area (A), solute concentration gradient (ΔC) and solute permeability (Ps) (42,43).

$$\mathrm{Mass}\mathrm{transfer}\mathrm{of}\mathrm{solute}(\mathrm{Js})=\mathrm{A}*\mathrm{\Delta C}*\mathrm{Ps}$$

In case of IP administration, the effective surface area (A) is created by the microvilli on mesothelial cells, which ensure increased absorption of IP administered substances. Because substances are efficiently carried away by capillary blood flow, a constant concentration gradient (ΔC) is available between the absorption site of the peritoneal cavity and surrounding capillaries. This concentration gradient facilitates the diffusion of administered substances from peritoneal cavity into blood capillaries. Lastly, physicochemical properties of the administered substance determine its permeability (Ps) and hence absorption from peritoneal cavity. A highly lipophilic substance has a higher distribution rate into tissues, which results in rapid removal of substance from the systemic circulation. The latter increases the concentration gradient between blood capillaries and peritoneal cavity, and leads to increased absorption rate of the substance after IP administration (44). Notably, solute permeability is the main determinant of convection rate, whereas concentration gradient is the main driving force for diffusion (45).

CAPILLARY ABSORPTION OF SOLUTES AFTER IP ADMINISTRATION

In the peritoneal microvascular network, majority of the solute and fluid exchange between peritoneal cavity and circulatory system occurs through capillaries. The capillary walls of the peritoneal capillaries are ‘continuous’ type, lined with single layer of continuous endothelial cells and basal lamina. These endothelial cells are very thin (0.5 μm) and highly permeable (46,47), plus they contain a large number of cytoplasmic vesicles (48–50). Intracellular clefts (6–7 nm thin channels located between adjacent endothelial cells) are also present in these capillaries which ensure rapid passage of water soluble ions and small molecules (21). Absorption of molecules with molecular size of <20,000 Da from peritoneal cavity occurs by either diffusion or convection through these capillaries (42,51). The rate and extent of diffusion depends on the size, charge, configuration and concentration gradient of the molecules (52). In addition, IP administration of a drug in solution increases the IP hydrostatic pressure which drives the convection of the soluble drugs along with fluid through peritoneum into the blood capillaries (45). Molecules absorbed from the visceral peritoneum, mesentery and omentum are drained into the portal vein, while molecules absorbed form the parietal peritoneal blood capillaries and lymphatics drains directly into the systemic circulation (53,54). Substances entering through portal circulation merge with systemic circulation after passing through liver which results in fast pass metabolism of the administered substances.

In one extensive experimental study carried out in rats, Lukas and colleagues have shown that after IP administration of small molecules (atropine, caffeine, glucose, glycine and progesterone), the primary route of absorption is through portal circulation (29). In this study the small molecules were selected to represent different physicochemical properties (basic, nonionic hydrophilic, zwitterionic and nonionic hydrophobic) and it was revealed that they all had comparable absorption pattern. In addition, the rate of absorption between IP and sub-cutaneous (SC) administrations of these compounds was compared. IP administered compounds could be detected in systemic circulation as soon as after 10 s of administration whereas it took about 60 s for SC administered compounds to reach systemic circulation. Another notable distinction between these two routs was the substantially lower degree of liver exposure and hence less biotransformation of molecules administered SC (29). Additionally, lipid solubility of IP administered compounds can affect the rate of their absorption. In general, increased lipid solubility leads to increased absorption from peritoneal cavity; e.g. only ~57.4% of barbital (lipid-water partition co-efficient of 0.001) was shown to be absorbed after IP administration in the rat, whereas absorption of thiopental (lipid-water partition co-efficient of 3.3) was shown to be 96.1% in the same study (55). Another important factor in absorption of IP-administered compounds is their ionization state at physiologic pH, which can be affected by buffering capacity of the peritoneal cavity (55). In general, absorption of IP-administered acidic substances increases as their pKa increases, e.g. benzyl penicillin with pKa of 2.8 has an absorption of 16.5%, whereas secobarbital with pKa of 7.9 has an absorption of 87% (55). On the other hand, absorption of IP-administered basic substances decreases as their pKa increases, e.g. caffeine with pKa of 0.9 has an absorption of 68.3%, whereas atropine with pKa of 9.6 has an absorption of 27% (55). Overall, unionized compounds are absorbed to a greater extent after IP administration than ionized compounds. Importantly, viscosity of the IP-administered formulations can also affect the absorption of pharmacological agents, with higher viscosity leading to decreased absorption and efficacy (55).

LYMPHATIC ABSORPTION OF SOLUTES AFTER IP ADMINISTRATION

Cellular arrangement around the peritoneum and ample supply of blood and lymph vessels assures rapid absorption of not only small molecules but also proteins and cells after IP administration (56,57). Molecules with molecular weight larger than 30,000 Da enter the systemic circulation from the peritoneal cavity primarily via lymphatic vessels (41). Experimental studies indicate that IP administered plasma proteins are completely absorbed into systemic circulation and are distributed throughout the body similar to IV administered plasma proteins (58). Following IP administration, proteins are absorbed by lymphatic vessels, which are especially enriched around the diaphragm in most mammals including mouse, rat, dog, cat and human (59,60). In addition to proteins, small particles and cells are also absorbed mainly through end lymphatic vessels, which are also known as stomata (61,62). The peritoneal stomata are physiological openings in the peritoneum. Here, the mesothelial cells are interrupted and share a common basement membrane with lymphatic endothelium which allows a direct communication between peritoneal cavity and underlying lymphatics (11). Notably, relaxation of the diaphragm during respiration also controls the absorption of macromolecules from the peritoneal cavity (63). The diaphragm relaxes during expiration and the adjacent mesothelial cells on the border of lacunae separate from each other creating suction force and facilitating absorption of macromolecules. However, contraction during inspiration results in closing of gaps between mesothelial cells and emptying of lacunae into the efferent lymphatics. The parasternal lymphatics located in the diaphragm, especially in the right half around the liver, are mainly responsible for the transfer of peritoneal deposits form peritoneal cavity into the mediastinal nodes and then into venous circulation through the right lymphatic duct (32,62). A small portion of peritoneal deposits are also drained through the paravertebral and mediastinal lymphatics situated on the parietal peritoneum, mesenteric, and omentum (60). The visceral lymphatics collect solutes and fluids from the omentum as well as mesentery and drain into the complex network of visceral lymph nodes. Subsequently, these visceral lymphatics collectively drain into parietal lymph nodes and finally dump the contents into venous circulation primarily through the thoracic duct (64). Quantitatively, about 75% of the absorbed proteins are drained into the right lymph duct and about 25% into the thoracic duct, which subsequently merge with venous circulation (Fig. 3) (57,65). Notably, obstruction of the right lymphatic and thoracic ducts does not prevent systemic absorption of proteins from the peritoneal cavity because trace amounts of proteins can still be absorbed through other small lympho-venous communications and capillary walls (60).

Fig. 3.

Schematic representation of the main lymphatic absorption pathways for macromolecules after IP administration.

PHARMACOKINETICS OF SMALL MOLECULES ADMINISTERED VIA IP VS OTHER ROUTES

Recently, Durk and colleagues carried out a comprehensive study in rats to compare the pharmacokinetic parameters of IP and SC administered 9 small molecules (carbamazepine, citalopram, desmethylclozapine, diphenhydramine, gabapentine, metaclopramide, naltrexone, quinidine and risperidone) with distinct physicochemical properties (66). For all molecules, administered at 1 mg/kg dose, IP administration yielded higher C_max and lower t_max values in comparison to the SC route (Table I). The authors also compared AUC_0–360 ratio of the brain interstitial fluid and plasma for all 9 molecules after IV infusion (1 mg/kg/h for 6 h) or 3 intermittent doses of IP or SC injections (2 mg/kg, every 2 h) (66–68). These experiments revealed that after IP administration, the brain to plasma ratios were greater than 1 for diphenhydramine and naltrexone, close to 1 for carbamazepine, metaclopramide and risperidone, and substantially less than 1 for citalopram, desmethylclozapine, gabapentin and quinidine. Notably, brain exposure of most compounds were higher after IP or SC administration in comparison to IV infusion which could be due to saturation of transporters at the blood brain barrier and rapid elimination rate after IV infusion (Table II).

Table I.

Pharmacokinetic Parameters of 9 Distinct Small Molecules After IP and SC Administration in the Rat (Tabulated from Data Reported in Durk et al., 2018)

Drug	MW*	Charge	Route	Cmax (ng/ml)	tmax (h)	t1/2 (h)
Carbamazepine	236	Neutral	SC	305 ± 132	0.41 ± 0.76	2.87 ± 2.09
			IP	426 ± 191	0.11 ± 0.98	0.74 ± 0.18
Citalopram	324	Basic	SC	95.6 ± 36.3	0.50 ± 0	1.17 ± 0.04
			IP	106 ± 67.1	0.36 ± 0.55	1.33 ± 0.61
Desmethylclozapine	313	Basic	SC	212 ± 62.3	1.17 ± 0	3.87 ± 1.35
			IP	268 ± 112	1.01 ± 0	2.83 ± 0.46
Diphenhydramine	255	Basic	SC	44.5 ± 21.9	0.50 ± 0.57	0.84 ± 0.33
			IP	38.7 ± 15.5	0.044 ± 0.28	0.90 ± 0.47
Gabapentine	171	Zwitter	SC	657 ± 127	1.67 ± 0.57	5.88 ± 2.44
			IP	1060 ± 305	0.833 ± 0.28	3.93 ± 1.15
Metaclopramide	300	Basic	SC	49.9 ± 17.2	0.50 ± 0	4.25 ± 6.1
			IP	74.8 ± 43.6	0.04 ± 0	0.61 ± 0.12
Naltrexone	341	Basic	SC	105 ± 30.3	0.41 ± 0.14	3.68 ± 5.43
			IP	128 ± 26.4	0.19 ± 0.26	1.16 ± 1.30
Quinidine	324	Basic	SC	84.7 ± 32.8	0.66 ± 0.28	0.99 ± 0.32
			IP	11 1 ± 65.5	0.11 ± 0.12	0.72 ± 0.24
Risperidone	410	Basic	SC	156 ± 68.9	0.66 ± 0.28	3.19 ± 3.35
			IP	169 ± 67.5	0.04 ± 0	0.72 ± 0.28

^*, molecular weight in g/mol; values are mean ± S.D.

Table II.

Comparison of Brain to Plasma AUC of 9 Distinct Small Molecules After IV, SC and IP Administration in the Rat (Tabulated from Data Reported in Durk et al., 2018)

Drug	AUC 0–360, ISF / AUC0–360, plasma
	IV infusion (1 mg/kg/h for 6 h)	Subcutaneous (2 mg/kg every 2 h × 3)	IP (2 mg/kg every 2 h × 3)
Carbamazepine	0.250 ± 0.07	0.779 ± 0.06	1.31 ± 0.23
Citalopram	0.438 ± 0.13	0.450 ± 0.28	0.467 ± 0.15
Desmethylclozapine	0.0902 ± 0.06	NC	0.098 ± 0.04
Diphenhydramine	2.24 ± 0.43	2.43 ± 0.95	3.38 ± 0.94
Gabapentine	0.0153 ± 0.01	0.0622 ± 0.01	0.0747 ± 0.02
Metaclopramide	0.0905 ± 0.02	0.646 ± 0.31	0.747 ± 0.13
Naltrexone	0.441 ± 0.16	1.55 ± 0.67	2.78 ± 0.65
Quinidine	0.154a	NC	0.143 ± 0.05
Risperidone	0.620a	0.776 ± 0.64	0.793 ± 0.20

Values are mean ± S.D. NC, not calculated in the original article.

^a, S.D. was not reported in the orignal article

Several other studies also compared pharmacokinetic properties of small molecular drugs administered via IP and other routs (Table III). Among them, a study carried out by Shimada and colleagues compared plasma and peritoneal concentrations of docetaxel (8 mg/kg, MW = 807.89) after IP and IV administration in mice (69). In intact mice, AUC of 4.85 and 3.37 mg h/ml were observed after IV and IP administration of the drug, respectively. Based on these data the calculated absolute bioavailability (F% = AUC IP/AUC IV × 100%) of IP administered docetaxel is 69% (69), which is much higher compared to the absolute bioavailability of docetaxel after oral administration (~2.8%) (70). Notably, the documented maximum plasma concentration (C_max) of docetaxel was also similar after IP and IV administration in this study.

Table III.

Pharmacokinetic Parameters of Various Small Molecules After IP and Other Routes of Administration in Rodents

Drug name	MW*	Route	Dose**	Pharmacokinetics			Ref.
				AUC***	Cmax #	t max ##
Docetaxel	807.879	IV	8	4850	1.2	NA	(69)
		IP	8	3370	1.2	1
Deramciclane	301.466	IV	10	3127.53	2643	NA	(71)
		IP	10	578.18	177.8	0.166
		Oral	10	106.95	44.94	0.5
Tariquidar (In DMSO)	646.73	IV	15	25,200	1.9	0.5	(73)
		IP	15	23,800	1.5	2
		Oral	15	18,100	1.2	4
Tariquidar (Microemulsion)	646.73	IV	15	25,200	1.9	0.5	(73)
		IP	15	25,600	1.6	2
		Oral	15	21,900	1.3	3.6
Lenalidomide	259.261	IV	10	284,000	158	NA	(74)
		IP	10	300,000	8.48	NA
		Oral	10	214,000	2.03	NA

^*, molecular weight in g/mol

^**, dose in mg/kg

^***, AUC in ng-h/ml

^#, t_max in h

^##, C_max in μg/ml

NA, not available

In another study, the plasma profile of deramciclane (10 mg/kg, MW = 301.466) was compared after oral, IP and IV administration in rats (71). Deramciclane showed AUC_0−∞ of 106.95, 578.18 and 3127.53 ng-h/ml after oral, IP and IV administration, respectively. The absolute bioavailability of the drug was almost 6-fold higher after IP vs oral administration. Furthermore, the time required to reach maximum plasma concentration of the drug was 4 times shorter after IP vs oral administration. Importantly, in case of both oral and IP routes of administration deramciclane had poor bioavailability due to heavy first pass metabolism in the liver.

One other study compared pharmacokinetic profile of IP vs oral or IV administered ¹⁸F-fluorodeoxyglucose (FDG, MW = 181.15 g/mol) for positron emission tomography/computed tomography (PET/CT) in mice (72). The authors concluded that the AUC and tissue uptake of FDG was greater in case of IP administration compared to the oral route. The time to reach maximum tissue concentration (t_max) was shorter after IP administration indicating a more rapid absorption of FDG after IP vs oral administration. Notably, the brain accumulation of FDG was not significantly different after IP or IV administration, however, it was lower after oral administration (72).

In another recent study, Matzneller and colleagues compared bioavailability of tariquidar (MW = 646.73 g/mol) at 15 mg/kg dose in two different formulations after oral, IP and IV administration in rats (73). For formulation A (tariquidar dissolved in 5% glucose and 2% DMSO solution), the AUC were 18.1 μg.h/ml, 23.8 μg.h/ml and 25.2 μg.h/ml after oral, IP and IV administration, respectively. Whereas, C_max were 1.2 μg/ml, 1.5 μg/ml, 1.9 μg/ml and t_max were 4 h, 2 h, and 0.5 h after oral, IP and IV administration, respectively. These parameters were further improved in formulation B (microemulsion of tariquidar), for which AUC were 21.9 μg.h/ml, 25.6 μg.h/ml and 25.2 μg.h/ml, C_max were 1.3 μg/ml, 1.6 μg/ml, 1.9 μg/ml and t_max were 3.6 h, 2 h, and 0.5 h after oral, IP and IV administration, respectively. Notably, for both formulations, the absolute bioavailability (F%) was higher after IP vs oral administration; for formulation A, F% was 71.6 and 91.4 after oral and IP administration, for formulation B, F% was 86.3 and 99.6, respectively.

In a similar study carried out in mice, it was revealed that IP administered lenalidomide (MW = 259.261 g/mol) has better bioavailability compared to oral administration (74). Administration of the drug at 10 mg/kg dose resulted in AUC of 214 μg.min/ml, 300 μg.min/ml and 284 μg.min/ml after oral, IP and IV administration, respectively. The absolute bioavailability (F%) was 75 and 105 after oral and IP administration, respectively. Whereas, the absorption rate was higher after IP vs oral administration, with an absorption constant (K_a) of 0.044 min⁻¹ and 0.014 min⁻¹, respectively.

In summary, these experimental studies indicate that IP administration of small molecule pharmacological agents results in faster and more complete absorption compared to oral and SC routes. Given the fast absorption of most substances from peritoneal cavity, it is generally considrered that systemic exposure (AUC and C_max) of a IP-admnistered substance is closer to that of the IV route. However, it is difficult to state how similar the exposure profiles are for the two routes, expecially considering that IP-administered substances are subject to first pass metabolism similar to orally administered substances (29,75). The uncertaininty is reasoned by a close examination of the published literature indicating that a good number of pharmacokinetic studies comparing IP and other routes, did not consider the rapid absorbtion of substances from peritoneal cavity and did the first blood sampling 30 min after IP administration (69,73,76). For rapidly absorbed compounds such experimental design could substantially underestimate systemic exposure of the pharmacological agent after IP administration, and provide an indication of higher first pass metabolism. Unfortunately, analysis of the published studies does not allow to unequivocally conclude whether the first pass metabolism of IP-administered small molecules is as extensive as in case of the oral route, and future studies specifically designed to answer this question will be needed to clarify the notion.

PHARMACOKINETICS OF MACROMOLECULES ADMINISTERED VIA IP VS OTHER ROUTES

Numerous in vivo studies conducted in various animal models of disease have shown biological effect(s) of macromolecules and recombinant proteins after IP administration indicating bioavailability of large molecules administered by this route (77–80). In addition, some studies focused on complete or partial pharmacokinetic characterization of macromolecules after IP administration providing more detailed information about suitability of this route for administration of macromolecules (Table IV).

Table IV.

Plasma Pharmacokinetic Parameters of Various Macromolecules After IV, IP and SC Routes of Administration in Rodents

I	MW (kDa)	Route	Dose	Pharmacokinetics			Ref.
				AUC*	C max*	t max
IgG-TNF	210	IV	10 mg/kg	10.8(0–1h)	~250	NA	(81)
		IP	10 mg/kg	94.52(0–24h)	120	6 h
		SC	10 mg/kg	17.23(0–24h)	20	6 h
rEpo	37	IP	5000 U/kg	140,331	10,015	3 h	(82)
		SC	5000 U/kg	117,677	6224	9 h
SOD	37	IV	4000 IU	1.20%a	300	NA	(83)
		IP	4000 IU	0.87%a	40	1.67 h
		IM	4000 IU	0.72%a	15	2.5 h
		SC	4000 IU	0.59%a	18	2.5 h
MPEG-SOD	42	IV	3000 IU	100%	300	NA	(83)
		IP	3000 IU	71%	100	10 h
		IM	3000 IU	54%	70	42 h
		SC	3000 IU	29%	62	40 h
Exedin-4	4.186	IV	50 nM	172	NA	NA	(84)
		IP	50 nM	128	35.3	1 h
		SC	50 nM	112	28	0.5 h
sIL-1R	68	IV	340 ng	NA	178	1 min	(85)
		IP	240 ng	NA	32	2h
		SC	240 ng	NA	14	4 h
sIL-4R	140	IV	1.1 μg	NA	1.2	2 min	(85)
		IP	1.1 μg	NA	0.19	1 h
		SC	1.1 μg	NA	0.21	1 h
AD-1 14-PA600-6H	60.6	IV	10 mg/kg	1871	467	1.8 min	(88)
		IP	10 mg/kg	1435	176	2 h
		SC	10 mg/kg	760	32.17	8 h
IFN-γ	16.8	IP	100 μg/kg	12.54	3.41	2 h	(89)
		SC	100 μg/kg	0.947	0.35	2 h
PEG-10- IFN-γ	~26	IP	100 μg/kg	3.30	160.03	4 h	(89)
		SC	100 μg/kg	1.12	15.62	>24 h
PEG-20- IFN-γ	~36	IP	100 μg/kg	6.4	179.5	4 h	(89)
		SC	100 μg/kg	2.3	29.52	>24 h
PEG-40- IFN-γ	~56	IP	100 μg/kg	28.25	567.29	10 h	(89)
		SC	100 μg/kg	2.12	23.47	>24 h
Anti-CD20 mAb	145	IP	150 μg	106.63	0.195	~24 h	(90)
		SC	150 μg	51.67	0.203	~24 h
phFVIII	90–200	IP	50 U/kg	NA	~300	2–4 h	(91)
		SC	50 U/kg	NA	#	NA
ohVWF	500–2000	IP	50 U/kg	NA	~250	2–4 h	(91)
		SC	50 U/kg	NA	#	NA
GLP-I	3297**	IP	50 nM	0.77	2.64	NA	(84)
		SC	50 nM	1.54	5.14	NA

^*Units for AUC and C_max are different among various macromolecules, however, they are the same within the same study for different routes of administration (see details in the text where the specific study is discussed).

^a, %AUC in comparison to AUC of IV administered MPEG-SOD.

^#, the protein was undetectable in plasma after SC administration.

NA, not available.

^**, MW in g/mol

In an elegant study conducted in mice, Sumbria and colleagues investigated plasma and brain availability of IgG-TNF Decoy Receptor Fusion Protein (MW = 210 kDa) after IV, IP and SC administration at 0.7, 3 and 10 mg/kg doses (81). The observed C_max values decreased in the following order IV > IP > SC for all three doses. The calculated plasma AUC for 10 mg/kg dose were 10.8 mg.min/mL, 94.521 mg.min/mL and 17.233 mg.min/mL for IV_0–1h, IP_0–24h and SC_0–24h routes, respectively, indicating a 5.5-fold higher AUC_0–24h after IP vs SC. Notably, while plasma concentrations of the noted groups were different, the brain concentrations were not different between IP and SC injections.

A recent comparative study carried out in neonatal rats evaluated the plasma and brain pharmacokinetics of recombinant human erythropoietin (rEpo, MW = 37 kDa, administered IP or SC at 5000 U/kg) (82). The calculated plasma AUC_0−∞ were 140,331 U.h/L, 117,677 U.h/L and brain AUC_0–24 were 52.5 U.h/L, 45.2 U.h/L after IP and SC administration, respectively. Plasma and brain C_max were 10,015 U/L and 3.3 U/g after IP administration, and 6224 U/L and 2.8 U/g after SC administration, respectively. Plasma t_max was 3 h for IP and 9 h for SC administration.

In another study, Veronese and colleagues studied bioavailability of intact superoxide dismutase (SOD, MW = 37 kDa; 4000 IU) and monomethoxypoly-ethylene glycol (MPEG) conjugated SOD (3000 IU) after IV, IP, intramuscular (IM) and SC administration in the rat (83). In case of MPEG-conjugated SOD, the calculated AUC were 71, 54 and 29% of the administered dose after IP, IM and SC administration (compared to IV route), indicating the following order of bioavailability IV > IP > IM > SC. The plasma C_max values were ~300 μg/ml, 100 μg/ml, 70 μg/ml and 62 μg/ml for IV, IP, IM and SC routes, whereas absorption rates decreased in following order IP > IM > SC, and t_max values were 10 h, 42 h and 40 h, respectively. In comparison to AUC of IV administered MPEG-conjugated SOD, the observed AUC of intact SOD after IV, IP, IM and SC administration were 1.20, 0.87, 0.72 and 0.59% indicating superior stability of the conjugated SOD over the intact form. The absorption rate of intact SOD was highest after IP administration, followed by IM and SC routes (IP > IM > SC), with t_max values of 100 min, 150 min and 150 min, respectively.

In another study, Parker and colleagues performed pharmacokinetic evaluation of Exendin-4 (a homolog of glucagon-like peptide-1 (7–36)amide, MW = 4186.63 Da) in rats (84). The observed AUC values were 172 ± 5 nM.h/ml, 128 ± 25 nM.h/ml and 112 ± 18 nM.h/ml following IV, IP and SC administration of 50 nmol Exendin-4. It was also revealed that IP administration results in higher C_max (35.3 ± 6.1 nM) compared to SC (28 ± 4 nM) administration, whereas elimination was also more rapid after IP (t_1/2 = 157 min) compared to SC (t_1/2 = 216 min) administration.

Additionally, pharmacokinetic parameters of radiolabeled soluble interlukin-1 receptor (IL-1R, MW = 68 kDa) were studied after IV (340 ng), IP (240 ng) and SC (240 ng) administration in mice (85). Though the study did not report AUC values, the observed C_max was 178 ng/mL, 32 ng/mL and 14 ng/mL, and t_max was 1 min, 120 min and 240 min after IV, IP and SC administration of IL-1R, respectively. In the same study, the authors studied pharmacokinetic properties of soluble interlukin-4 receptor (IL-4R, MW = 140 kDa at 1.1 μg). For IL-4R the observed C_max was 1.2 μg/mL, 0.19 μg/mL, 0.21 μg/mL, and t_max was 2 min, 60 min, 60 min after IV, IP and SC, respectively.

To study the effect of dose and injection volume on pharmacokinetics of IP administered macromolecules, Barrett and colleagues injected two doses (2 and 100 μg) of IgG2_ak (IgG light chain, MW = 25 kDa) at two different injection volumes (2 and 20 ml) in rats (86). Their observations revealed that higher dose of administered IgG2_ak results in higher AUC and C_max whereas, the higher volume resulted in lower AUC and C_max. According to the authors and another research group (87), IP injection of higher volume induces diuresis and increased clearance of the drug leading to a lower AUC.

In another study, comparative pharmacokinetics of AD-114-PA600–6H (human single domain antibody against CXCR4, MW = 60.6 kDa) at 10 mg/kg dose was studied in mice after IV, IP and SC administration (88). The results indicated higher AUC_last after IP administration compared to the SC, though the highest AUC was observed after IV administration; AUCl_ast for IV, IP and SC were 1871 μg.h/mL, 1435 μg.h/mL and 760 μg.h/mL, respectively. The C_max were 467 μg/mL, 176 μg/mL and 32.17 μg/mL with t_max values of 1.8 min, 2 h and 8 h for IV, IP and SC administration of AD-114-PA600–6H, respectively.

A comprehensive pharmacokinetic study of IFN-γ (MW = 16.8 kDa, 100 μg/kg) and its PEG-ylated conjugates (with PEG-10, −20 and − 40 at 100 μg/kg dose) in rats showed higher AUC_0–∞ and C_max values after IP vs SC administration for all IFN-γ forms (89). In addition, the observed t_max after IP administration was 4 h, 4 h, 10 h and 2 h for PEG-10, PEG-20, PEG-40-conjugated and intact IFN-γ, respectively, whereas it exceeded 24 h for all PEG-ylated IFN-γ and was 2 h for native IFN-γ after SC administration. C_max values were 160.03 ng/mL, 179.50 ng/mL, 567.29 ng/mL and 3.41 ng/mL after IP, and 15.62 ng/mL, 29.52 ng/mL, 23.47 ng/mL and 0.35 ng/mL after SC administration for PEG-10, PEG-20, PEG-40-conjugated and intact IFN-γ, respectively.

In another study, pharmacokinetics of anti-CD-20 monoclonal antibody veltuzumab (MW = 145 kDa, at 150 μg) was studied in mice after IP and SC administration (90). The calculated AUC was 106.639 nmole.h/mL after IP and 51.67 nmole.h/mL after SC administration. The observed C_max were 0.195 and 0.203 nmole/mL for IP and SC administration, whereas t_max was ~24 h for both routes.

In a recent study Shi and colleagues examined suitability of IP and SC routes, in comparison to IV, for administration of large plasma-derived proteins, coagulation factor VIII (phFVIII, MW = 90–200 kDa, 50 U/kg) and von Willebrand factor (phVWF, MW = 500–2000 kDa, 50 U/kg) in mice (91). Both proteins were absorbed with t_max of 2 to 4 h after IP administration, with observed C_max of ~250 mU/mL for phVWF and ~300 mU/mL for phFVIII, which is similar to plasma level of these proteins 2 to 4 h after IV administration. On the contrary, phVWF and phFVIII were undetectable after SC administration in mice, even though another coagulation factor with a smaller molecular size (FIX, MW = 55 kDa) was shown to be absorbed in significant amounts after SC administration in another study (92). Notably, Shi and colleagues concluded that the hindered absorption of phVWF and phFVIII after SC was likely due to their large molecular size retarding absorption through subcutaneous capillaries and lymphatics.

It is noteworthy, that not all studies documented better pharmacokinetic profile of IP vs SC administered ploypeptides or proteins. For example, in the study where Parkes and colleagues observed higher AUC of exendin-4 after IP vs SC administration, pharmacokinetics of glucagon-like peptide-1 (7–36) amide (also known as GLP-1) was also studied in the rat (84). Their observations revealed lower AUC for GLP-1 after IP vs SC administration, documenting AUC of 0.77 ± 0.16 nM.h/ml and 1.54 ± 0.24 nM.h/ml, respectively. Additionally, C_max after IP and SC administration of 50 nmol GLP-1 were 2.64 ± 2.11 nM and 5.14 ± 1.16 nM, respectively. The authors attributed these results to potential biodegradation of GLP-1 upon absorption from peritoneal cavity (84).

Collectively, based on the above-discussed experimental studies, we can suggest that macromolecules of different molecular size get access to systemic circulation after IP administration in intact/therapeutically active form and, in majority of cases, systemic exposure of these molecules, i.e. AUC, is higher after IP than SC route of administration (summarized in Table IV).

BIOAVAILABILITY OF SUSPENSION AND NANOPARTICLE FORMULATIONS ADMINISTERED VIA IP ROUTE

In addition to solution formulations of small and macromolecules discussed above, experimental studies point out to bioavailability of suspension formulations after IP administration. Absorption of suspension preparations after IP administration is mainly through lymphatic system and is primarily affected by physicochemical properties of the pharmacological agent, dissolution rate of the suspension in the peritoneal cavity and particle size (93). For example, in a recent study Cardenas and colleagues studied systemic bioavailability of 6-methylcoumarin (water insoluble, MW = 160.17 g/mol) in rats after IP and oral administration of 200 mg/kg suspension prepared in Tween-80 and saline (94). The authors observed more rapid absorption and higher bioavailability of the suspension after IP vs oral administration, documenting t_max values of 6 min and 30 min, and AUC of 2177.0 μg.min/ml and 977.2 μg.min/ml, respectively. On the other hand, systemic bioavailability of 100 mg/kg elacridar suspension (water insoluble, MW = 563.6 g/mol), prepared in hydroxypropyl-methylcellulose and Tween-80, after IP administration in mice was several fold lower compared to that of oral administration, with AUC of 90.30 μg.min/ml and 1460 μg.min/ml, respectively (95). Notably, when the same drug was given as a microemulsion (prepared with Cremophor EL, Carbiton and Captex 355) at 10 mg/kg, systemic bioavailability of the formulation after IP administration was several times higher compared to oral administration, with AUC of 962 μg.min/ml and 270 μg.min/ml, respectively (76). The authors concluded that lower bioavailability of elacridar suspension compared to emulsion was due to lower dissolution of the administered formulation in the peritoneal cavity, which contains smaller amount of fluid compared to the gastrointestinal tract. It is noteworthy, that dissolution of the suspension formulation can be improved by vehicle selection. For instance, Sofia and colleagues have compared the influence of different suspension vehicles on central effects of Δ9-tetrahydrocannabinol (water insoluble, MW = 314.45 g/mol) at 10 and 40 mg/kg doses after IP administration (96). Among four different vehicles studied (bovine serum albumin-saline (BSA), 1% Tween-80-saline, polyvinylpyrolidone-saline (PVP) and 10% propylene glycol-1% Tween 80-saline (PG)), suspension of Δ9-tetrahydrocannabinol in PG was the most effective followed by PVP suspension. In a subsequent study, the same investigators studied suspensions of Δ9-tetrahydrocannabinol in the same four vehicles after IV, IP, oral, and SC administration (97). The strongest CNS effects were observed with PG suspension and the effects descended in the following order IV > IP > SC > oral, based on the route of administration (97). Lastly, particle size of the suspension formulation can also affect the efficacy of IP administered drugs. The latter was demonstrated by Ritschel and colleagues who studied toxicity of pentobarbiturate suspension in 1% sodium-carboxymethyl cellulose at two different particle sizes (<44 μm and 297–420 μm) administered IP in mice, and observed about twice higher toxicity of the drug at small vs large particle size suspension (LD50 of 189 and 288 mg/kg, respectively) (98). Another recent study investigated pharmacokinetics of two poorly water soluble substances (at 5 μmol/kg, referred to as AC88 and BA99) after IP administration in the rat, in the form of microsuspension (prepared with hydroxylpropyl-methylcellulose) and nanosuspension (prepared with Aerosol OT, polyvinylpyrolidone and mannitol) (99). For both substances nanosuspensions showed about twice higher AUC compared to that of microsuspensions. More specifically, the observed C_max, t_max and AUC values were 8.24 μmol/L, 3 h and 136 kg.h/L for AC88 microsuspension (mean size 14 μm), and 21.2 μmol/L, 2 h and 233 kg.h/L for AC88 nanosuspension (mean size 219–251 nm). Similarly, for BA99 microsuspension (mean size 12 μm) the observed C_max, t_max and AUC values were 10.4 μmol/L, 0.7 h and 50.6 kg.h/L, whereas for BA99 nanosuspension (mean size 291 nm) the observed values were 20.1 μmol/L, 0.31 h and 85.4 kg.h/L, respectively (99). Notably, the same research group studied bioavailability of AC88 and BA99 nanosuspensions after oral and SC administration in the rat (at 5 μmol/kg) in two parallel studies, and reported ~5–8 fold lower AUC values compared to IP administration of the same nanosuspensions (100,101).

It is important to note, that while the small particle size of nanoformulations facilitates enhanced absorption of pharmacological agents, encapsulation of active substances in nanoformulations often results in decreased clearance from systemic circulation and ultimately higher drug exposure. In addition, depending on specifics of nanocapsulated formulation release of the drug may also be prolonged leading to higher drug exposure. For example, pharmacokinetic comparison of lipid core nanocapsule formulation of olanzapine (sparingly water soluble, MW = 312.4 g/mol) with free olanzapine after IP administration (at 10 mg/kg) indicated ~2.3 fold increased bioavailability of the nanoformulation in the rat (102). In addition, higher C_max and lower clearance (CL) values were observed for olanzapine nanoformulation (3.02 μg/ml and 1.36 L/h/kg) compared to the free drug (1.12 μg/ml, and 3.12 L/h/kg). And because the observed absorption rate was comparable for both formulations (tmax ~1 h) the authors concluded that the observed higher bioavailability of nanoformulation was largely due to decreased CL (103). In another study, chitosan-coated PLGA nanoparticles of docetaxel (sparingly water soluble, MW = 807.87 g/mol) were studied in the rat after IP administration (at 13 mg/kg) and ~4.7 fold higher bioavailability of the drug was observed for the nanoparticle formulation in comparison to free docetaxel suspension (103). Notably, the time to reach maximum plasma concentrations (2 and 0.5 h) as well as the elimination half-life (5.2 and 2.6 h) were higher for the nanoformulation, indicating overall longer residence time for docetaxel nanoparticle (7.4 h) in comparison to the free form (4.3 h) (102). Similarly, in a recent study Ragelle and colleagues studied bioavailability of free (at 223 mg/kg) and nanoemulsion (at 112.5 mg/kg, prepared with Miglyol® 812 N, Labrasol®, Tween-80, Lipoid® E80 and water) fisetin (sparingly water soluble, MW = 286.23 g/mol) after IP administration in the rat (104). Their observations indicate that bioavailability of fisetin nanoemulsion was about 24 fold higher compared to the free drug, and it had to do with more rapid absorption (1.97 and 5.98 h) and lower clearance (2.32 and 54.8 L/kg/h) of the nanoemulsion vs free drug, respectively (104).

In summary, these experimental studies suggest that drugs in suspension and/or nanoparticle formulations also reach systemic circulation after IP administration. Notably, the physicochemical properties of the drug, dissolution rate of the suspension in the peritoneal cavity and particle size critically affect absorption rate and bioavailability of the administered drug. In general, higher dissolution rate and smaller particle size lead to more complete and rapid absorption of such formulations from peritoneal cavity and result in higher bioavailability. From the other hand, slow dissolution rate may lead to more prolonged absorption of the drugs from such formulations and also result in longer exposure. Lastly, encapsulation of active substances in nanoformulations may prolong release of the pharmacological agent into systemic circulation, and often leads to decreased clearance of the drug.

LIMITATIONS OF THE IP ROUTE

Eventhough IP administration of pharmacological agents results in faster and more complete absorption compared to oral, intramuscular and SC routes, this route as any other, has certain limitations. One limitation is the first pass metabolism, similar to what is observed with orally administered drugs, because substances absorbed from the peritoneal cavity end up in portal vein and pass through the liver. It is generally considered that, pharmacokinetics of small molecular drugs administered through the IP route resemble that of orally administered drugs in terms of metabolic fate and high rate of first pass metabolism, which leads to lower systemic exposure of IP-administered substances (29,75). Notably, published literature does not allow to conclusively say whether the first pass metabolism of IP-administered sustances is as expensive as in case of the oral route and future studies will likely adress this question. On the contrary, IP administered macromolecules, which reach systemic circulation through lymphatic vessels, were shown to be minimally affected by first pass metabolism. This was well-documented with a number of recombinant enzymes including neurolysin (80), angiotensin converting enzyme 2 (105) and SOD (83) which retained catalytic activity upon reaching systemic circulation after IP administration in rodents.

Two other important considerations for IP administered agents include sterility and non-irritability, because irritating compounds may cause ileus and peritoneal inflammation, which may further develop into adhesions (106). Importantly, position of IP injection can aslo affect the absorption rate of substances. Although, not studied in experimental animals, a study carried out in humans showed that the time to reach maximum plasma concentration of insulin in healthy volunteers varied about 2-fold upon administration of the agent at a position above vs below the transverse mesocolon (107). The technique of injection and its accuracy may also affect the outcome of IP administration. One common mistake associated with IP drug admnistration (~20% of cases) is puncturing the skin at a very sharp angle which results in SC administration rather than IP (108). Although occurring less frequently, inaccurate IP administration may also deposit drugs into the gastrointestinal tract, retroperitoneum or the urinary bladder (109). Another important factor is the volume of IP administered drugs because large volumes (>10 ml/kg in rodents) can lead to pain, chemical peritonitis, formation of fibrous tissue, perforation of abdominal organs, hemorrhage, and respiratory distress (86,110,111). Repeated IP administration can result in a cumulative irritant effect and needle-induced damage of the peritoneum (5). Temperature of the IP administered solutions can also affect local absorption rate (112,113), whereas, hypothermia and distress can be observed if a large volume of a cold substance is administered IP (114,115).

CONCLUDING REMARKS

Proper formulation of a drug and appropriate route of administration are crucial for clinical success at later stages of drug development. However, such questions are usually addressed after proof-of-concept studies where the goal is to evaluate the effect(s) of target engagement rather than properties of a drug formulation and/or its pharmacokinetics for clinical translation. Because of these reasons, in exploratory as well as early preclinical studies it is more practical to choose a route of drug administration that ensures bioavailability of the drug and meets the needs of a specific experiment/scientific question rather than focuses on clinically applicable administration route. In this regard, IP route of administration can be the choice for in vivo experimental studies in rodents, because it is safe for animals, ensures therapeutic bioavailability of both small and large molecules, amendable to variety of formulations, suitable for chronic treatments, robust and easy to master.

Among all routes of drug administration the IV route usually results in the highest bioavailability of a drug. However, this route is often impractical for rodent studies, because most investigational pharmacological agents are difficult to fully dissolve in water/aqueous solutions (hydrophobic nature), it requires advanced skills to practice (especially in mice, due to small vessels), and is not well-suited for chronic/repetitive treatments. To avoid these problems, researchers often prefer administration of pharmacological agents through oral, IP or SC routes, all of which have certain advantages and disadvantages (summarized in Table V). Among these, the IP route stands out because the rate and extent of drug absorption is faster in IP followed by intramascular > SC > oral routes (116), and it is suitable for both drug solutions and suspensions/emulsions. This is primarily because IP administered pharmacological agents are exposed to a large surface area (close to that of the entire skin surface) which leads to rapid and efficient absorption. Notably, in majority of cases the effect elicited by a pharmacological agent after IV administration can be approximated more closely with IP rather than intramuscular or SC administration. Usually, the rate of absorption after IP administration is one-half to one-fourth as rapid as after IV administration (66,69,117). Following rapid absorption from the peritoneal cavity, a compound may face one of the following two pathways to reach systemic circulation: (1) it is absorbed through the visceral peritoneum, the mesentery and omentum and is drained into portal circulation, or (2) the compound gets into the systemic circulation directly bypassing liver when it is absorbed through parietal peritoneum and lymphatics. Notably, small molecular weight compounds are primarily absorbed through the first pathway, because the surface area of membranes transporting substances into the portal circulation is much larger (29,118). On the contrary, macromolecules access systemic circulation through the second pathway (lymphatics), which is very efficient but relatively less recognized among researchers.

Table V.

Brief Comparison of Different Routes of Drug Administration in Laboratory Rodents

IP route
Advantages	Disadvantages
Convenient and easy to master  Less stressful/harmful for animals  Suitable for variety of formulations (i.e., amendable to physicochemical properties of a drug)	High first pass metabolism  Need for sterility  Abdominal organs can be injured if done incorrectly
Peritoneal cavity has buffering capacity  Large volumes can be administered  Higher absorption rate  Suitable for repeated administrations  Suitable for administration of macromolecules	Limited clinical applicability
Oral Route
Advantages	Disadvantages
Convenient and easy to master  Suitable for repeated administrations  Large volumes can be administered  Clinically applicable	Can be stressful for animals  Can damage the esophagus  Low absorption rate and poor bioavailability  Food and pH may affect absorption  High first pass metabolism  Gut flora may contribute to metabolism  Usually not suitable for biological agents
Intravenous Route
Advantages	Disadvantages
No limitation in absorption  Buffering capacity is present  Rapid onset of action  Suitable for administration of macromolecules  Clinically applicable	Isotonic solution of a drug is required  Need for sterility  Technically challenging  Can be stressful for animals  Not suitable for large volume administration  Challenging for repeated administrations
Subcutaneous Route
Advantages	Disadvantages
Convenient and easy to master  Less stressful/harmful for animals  Suitable for most macromolecules  Clinically applicable	Low absorption rate and poor bioavailability  Not suitable for large volume administration  Local irritability  Need for sterility

Another important point of consideration is the suitability of IP route for chronic/repetitive treatments. For example, studies have shown that chronic IP administration (daily saline injection over 30 days in the same position of the abdomen) and use of different types of injection vehicles and volumes are safe and well-tolerated in laboratory animals (119,120).

From a technical standpoint, IP administrations is more reproducible and easy to master compared to other available routs, and upon mastering it is less stressful and safer for rodents.

Among main deficiencies of the IP route, is the metabolic fate of IP administered small molecular agents, which resembles that of the orally administered drugs (121). This may present a problem for pharmacological agents prone to extensive first-pass metabolism.

In summary, based on the knowledge discussed in this manuscript we conclude that IP administration of drugs in experimental studies involving rodents is a justifiable route for initial pharmacological and proof-of-concept studies where the goal is to evaluate the effect(s) of target engagement rather than properties of a drug formulation and/or its pharmacokinetics for clinical translation.