Enhanced oral bioavailability and intestinal lymphatic transport of a hydrophilic drug using liposomes

Sharon Sheue Nee Ling, Enrico Magosso, Nurzalina Abdul Karim Khan, Kah Hay Yuen, Susan Anne Barker

Research output: Contribution to journalArticlepeer-review

71 Citations (Scopus)

Abstract

A liposome system was evaluated for oral delivery of a poorly bioavailable hydrophilic drug. The system was prepared from proliposome, which consisted of negatively charged phosphatidylcholine, whereas cefotaxime was chosen as the model drug. An in vivo study was carried out on nine rats according to a three-way crossover design to compare the oral bioavailability of cefotaxime from the liposomal formulation with that of an aqueous drug solution and a physical mixture of cefotaxime with blank liposomes. The results indicated that the extent of bioavailability of cefotaxime was increased approximately 2.7 and 2.3 times compared with that of the aqueous solution and the physical mixture, respectively. In a separate study, simultaneous determination of cefotaxime in intestinal lymph ( collected from the mesenteric lymph duct) and in plasma ( collected from the tail vein) revealed that its concentration was consistently higher in the lymph than in the plasma when administered via the liposomal formulation, whereas the reverse was observed with the aqueous solution. Thus, the results indicated that the liposomes system has the potential of increasing the oral bioavailability of poorly bioavailable hydrophilic drugs and also promote their lymphatic transport in the intestinal lymph.
Original languageEnglish
Pages (from-to)335-345
Number of pages11
JournalDrug Development and Industrial Pharmacy
Volume32
Issue number3
DOIs
Publication statusPublished - 2006

Cite this