DESIGN AND DEVELOPMENT OF SELF EMULSIFYING DRUG DELIVERY SYSTEM OF MARAVIROC

Journal Title: World Journal of Pharmaceutical Research - Year 2019, Vol 8, Issue 8

Abstract

Self emulsifying drug delivery systems (SEDDS) are isotropic mixtures of natural or synthetic oils, solids or liquid surfactants or alternatively, one or more hydrophilic solvents, and co-solvents or co-surfactants Maraviroc SEDDS formulation when diluted with 250 times gives globule size of 110 nm and zeta potential of -5.18. There is no significant difference in globule size when diluted with medias like 0.1 N HCl and Phosphate buffer of pH 6.8). Maraviroc drug release from the SEDDS formulation was performed in 0.1 N HCl and 87.92 (± 4.78) % released within 15 minutes. In-vitro drug diffusion study in dialysis membrane showed that 80.56 ± 2.81% maraviroc diffused from the SEDDS formulation in the Phosphate buffer of pH 7.4 in five hours, whereas only 42.86 (±2.12) % released from Maraviroc suspension at the same conditions. Maraviroc SEDDS formulation can be used in the treatment of AIDS.

Authors and Affiliations

Patel Rajendra

Keywords

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  • EP ID EP672871
  • DOI -
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How To Cite

Patel Rajendra (2019). DESIGN AND DEVELOPMENT OF SELF EMULSIFYING DRUG DELIVERY SYSTEM OF MARAVIROC. World Journal of Pharmaceutical Research, 8(8), 263-275. https://europub.co.uk/articles/-A-672871