| Literature DB >> 18826299 |
Eunhye Lee1, Jinju Lee, In-Hyun Lee, Mikyung Yu, Hyungjun Kim, Su Young Chae, Sangyong Jon.
Abstract
A new platform for oral delivery of paclitaxel (PTX) was developed through chemical conjugation of PTX to a low molecular weight chitosan (LMWC). The LMWC-PTX conjugate contained approximately 12 wt % PTX and showed greatly enhanced water solubility (>1 mg/mL) as compared to native PTX. The conjugate showed comparable IC 50 values to that of the parent PTX against human cancer cell lines. The pharmacokinetic data revealed approximately 42% of bioavailability after oral administration of 5 mg PTX/kg of the conjugate. When the conjugate (10 mg/kg based on PTX content) was administered orally to mice bearing xenograft or allograft tumors, the conjugate-treated group showed significant inhibition of tumor growth, which was comparable to that seen with PTX of the clinically available injected form, formulated in cremophor EL/ethanol (iv) but with much lower toxicity. Tracking I (125)-labeled conjugate showed that LMWC-PTX was likely to be absorbed mainly from the ileum and reach the blood as the intact conjugate.Entities:
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Year: 2008 PMID: 18826299 DOI: 10.1021/jm800767c
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446