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  • In vivo Evaluation of Self Emulsifying Drug Delivery System for Oral Delivery of Nevirapine.

In vivo Evaluation of Self Emulsifying Drug Delivery System for Oral Delivery of Nevirapine.

Indian journal of pharmaceutical sciences (2014-07-19)
A S Chudasama, V V Patel, M Nivsarkar, Kamala K Vasu, C J Shishoo
ABSTRACT

Nevirapine is a highly lipophilic and water insoluble non-nucleoside reverse transcriptase inhibitor used for the treatment of HIV-1 infection. Lymphoid tissue constitutes the major reservoir of HIV virus and infected cells in HIV-infected patients. Self-emulsifying drug delivery system, using long chain triglycerides, is a popular carrier of drugs due to their ability to transport lipophilic drugs into the lymphatic circulation. However, HIV/AIDS patients experience a variety of functional and anatomical abnormalities in gastrointestinal tract that result in diarrhoea and nutrient malabsorption. Medium chain triglycerides are readily absorbed from the small bowel under conditions in which the absorption of long chain triglycerides is impaired. Therefore, nevirapine self-emulsifying drug delivery system containing medium chain fatty acid, caprylic acid and a solubilizer, Soluphor(®) P (2-pyrrolidone) was developed and found to be superior to the marketed conventional suspension with respect to in vitro diffusion and ex vivo intestinal permeability. This self-emulsifying drug delivery system has now been further investigated for in vivo absorption in an animal model. The contribution of caprylic acid and Soluphor(®) P on in vivo absorption of nevirapine was also studied in the present study. The bioavailability of nevirapine from self-emulsifying drug delivery system, after oral administration, was 2.69 times higher than that of the marketed suspension. The improved bioavailability could be due to absorption of nevirapine via both portal and intestinal lymphatic routes. The study indicates that medium chain or structured triglycerides can be a better option to develop self-emulsifying drug delivery system for lipophilic and extensively metabolised drugs like nevirapine for patients with AIDS-associated malabsorption.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Octanoic acid, ≥96.0%
Sigma-Aldrich
Octanoic acid, ≥99%
Supelco
Octanoic acid, analytical standard
Sigma-Aldrich
Octanoic acid, ≥98%, FG
Sigma-Aldrich
Octanoic acid, ≥98%
Sigma-Aldrich
Octanoic acid, natural, ≥98%, FG
Pyrrolidone, European Pharmacopoeia (EP) Reference Standard
Supelco
Caprylic Acid (Octanoic Acid), Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
2-Pyrrolidinone, purum, ≥98.0% (GC)
Sigma-Aldrich
2-Pyrrolidinone, ≥99%
Sigma-Aldrich
2-Pyrrolidinone, 99%
Caprylic acid, European Pharmacopoeia (EP) Reference Standard