What is it called when drugs are administered through the veins of an animal?

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 []. 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 [,,]. Large volumes of solution [up to 10 ml/kg] can be safely administered to rodents through this route [] 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 []. 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 [], whereas in mice its volume ranges between 0.02 and 0.1 ml []. 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 [].

Peritoneum covers most of the intra-abdomenal organs and consists of a single layer of squamous mesothelial cells []. 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 []. The sub-mesothelial layer of peritoneum contains collagen, adipose tissue, lymphocytes, blood vessels as well as lymphatics []. Fibroblasts and occasional macrophages are also present in this part of the peritoneum []. 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. ] [].

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.

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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 [,]. 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 []. The peritoneal fluid has a pH of 7.5–8.0 and buffering capacity [], because of which substances are rarely ionized in the peritoneal cavity after IP administration [].

Peritoneal Blood Flow

The sub-mesothelial layer of the peritoneum supports a complex but efficient vascular network of blood and lymphatic vessels [,]. Most of the circulatory vessels are blood capillaries but few arterioles and venules are also present in the sub-mesothelium []. 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 [,]. Through these capillaries, peritoneal cavity receives 4 to 7% of the total cardiac output in the rabbit [] and rat [,]. The average peritoneal blood flow rate in the rat is 2.5–6.2 ml/min/kg []. 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 [,]. 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 [,]. 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 [].

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 [,]. 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 [].

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 [,]. Additionally, lymphatic transport of substrates significantly contributes to the total transfer from the peritoneal cavity to systemic circulation [].

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 [,]. 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. ] [].

Experimental studies indicate that small to medium size molecules [MW  5000], proteins, blood and immune cells are taken up by the lymphatics [Fig. ] []. 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 [,].

Fig. 2

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

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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] [,].

$$ \mathrm{Mass}\ \mathrm{transfer}\ \mathrm{of}\ \mathrm{solute}\ \left[\mathrm{Js}\right]=\mathrm{A}\ast \Delta \mathrm{C}\ast \mathrm{Ps} $$

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 []. Notably, solute permeability is the main determinant of convection rate, whereas concentration gradient is the main driving force for diffusion [].

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 [,], plus they contain a large number of cytoplasmic vesicles [,,]. 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 []. Absorption of molecules with molecular size of  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 IV0-1h, IP0–24h and SC0–24h routes, respectively, indicating a 5.5-fold higher AUC0–24h 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] []. The calculated plasma AUC0-∞ were 140,331 U.h/L, 117,677 U.h/L and brain AUC0–24 were 52.5 U.h/L, 45.2 U.h/L after IP and SC administration, respectively. Plasma and brain Cmax 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 tmax 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 []. 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 Cmax 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 tmax 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 tmax 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 [,,,,,,,,,,,,,,,,,,,,,,,,,,,,,]amide, MW = 4186.63 Da] in rats []. 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 Cmax [35.3 ± 6.1 nM] compared to SC [28 ± 4 nM] administration, whereas elimination was also more rapid after IP [t1/2 = 157 min] compared to SC [t1/2 = 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 []. Though the study did not report AUC values, the observed Cmax was 178 ng/mL, 32 ng/mL and 14 ng/mL, and tmax 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 Cmax was 1.2 μg/mL, 0.19 μg/mL, 0.21 μg/mL, and tmax 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 IgG2ak [IgG light chain, MW = 25 kDa] at two different injection volumes [2 and 20 ml] in rats []. Their observations revealed that higher dose of administered IgG2ak results in higher AUC and Cmax whereas, the higher volume resulted in lower AUC and Cmax. According to the authors and another research group [], 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 []. The results indicated higher AUClast after IP administration compared to the SC, though the highest AUC was observed after IV administration; AUClast for IV, IP and SC were 1871 μg.h/mL, 1435 μg.h/mL and 760 μg.h/mL, respectively. The Cmax were 467 μg/mL, 176 μg/mL and 32.17 μg/mL with tmax 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 AUC0-∞ and Cmax values after IP vs SC administration for all IFN-γ forms []. In addition, the observed tmax 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. Cmax 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 []. The calculated AUC was 106.639 nmole.h/mL after IP and 51.67 nmole.h/mL after SC administration. The observed Cmax were 0.195 and 0.203 nmole/mL for IP and SC administration, whereas tmax 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 []. Both proteins were absorbed with tmax of 2 to 4 h after IP administration, with observed Cmax 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 []. 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 [,,,,,,,,,,,,,,,,,,,,,,,,,,,,,] amide [also known as GLP-1] was also studied in the rat []. 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, Cmax 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 [].

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 ].

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 []. 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 []. The authors observed more rapid absorption and higher bioavailability of the suspension after IP vs oral administration, documenting tmax 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 []. 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 []. 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 []. 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 []. 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 []. 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 [10 ml/kg in rodents] can lead to pain, chemical peritonitis, formation of fibrous tissue, perforation of abdominal organs, hemorrhage, and respiratory distress [,,]. Repeated IP administration can result in a cumulative irritant effect and needle-induced damage of the peritoneum []. Temperature of the IP administered solutions can also affect local absorption rate [,], whereas, hypothermia and distress can be observed if a large volume of a cold substance is administered IP [,].

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 ]. 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 [], 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 [,,]. Following rapid absorption from the peritoneal cavity, a compound may face one of the following two pathways to reach systemic circulation: [] it is absorbed through the visceral peritoneum, the mesentery and omentum and is drained into portal circulation, or [] 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 [,]. 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

Full size table

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 [,].

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 []. 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.

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ACKNOWLEDGMENTS AND DISCLOSURES

Dr. Karamyan is supported by NIH [1R01NS106879] and AHA [14BGIA20380826] grants. We apologize that the scope of this manuscript prevented citation of all published experimental studies where the IP route of drug administration was used.

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Authors and Affiliations

1. Department of Pharmaceutical Sciences, School of Pharmacy, TTUHSC, Amarillo, Texas, USA

   Abdullah Al Shoyaib & Vardan T. Karamyan

2. Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Dhaka, Dhaka, Bangladesh

   Sabrina Rahman Archie

3. Center for Blood Brain Barrier Research, School of Pharmacy, TTUHSC, 1300 Coulter St., Amarillo, Texas, 79106, USA

   Vardan T. Karamyan

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Al Shoyaib, A., Archie, S.R. & Karamyan, V.T. Intraperitoneal Route of Drug Administration: Should it Be Used in Experimental Animal Studies?. Pharm Res 37, 12 [2020]. //doi.org/10.1007/s11095-019-2745-x

What method of administration when the drug is injected directly into the vein?

What are the routes of drug administration in animals?

What is it called when drugs are administered through the veins of an animal responses?

Which route of drug administration is into a vein?