1. Enhancing oral delivery and anticancer efficacy of 7-ethyl-10-hydroxycamptothecin through self-assembled micelles of deoxycholic acid grafted N'-nonyl-trimethyl chitosan.
- Author
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Huang, Jie, Tang, Xiao, Yang, Ziqiong, Chen, Jianqiu, Wang, Kun, Shi, Chengnan, Liu, Zihan, Wu, Ming, and Du, Qian
- Subjects
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IRINOTECAN , *DEOXYCHOLIC acid , *ANTINEOPLASTIC agents , *CHITOSAN , *MICELLES , *TRANSCYTOSIS - Abstract
Irinotecan (CPT-11) is used as a first or second-line chemotherapy drug for the treatment and management of colorectal cancers. In vitro studies have shown that 7-ethyl-10-hydroxycamptothecin (SN38), the active metabolite of CPT-11, displays promising anticancer efficacy. However, its poor aqueous solubility and hydrolytic degradation result in its lower oral bioavailability and impracticable clinical application. To overcome these limitations, a novel amphiphilic chitosan derivative, deoxycholic acid decorated N'-nonyl-trimethyl chitosan, was synthesized. Nano-micelles loaded with SN38 were subsequently prepared to enhance the bioavailability and anti-tumor efficacy of the drug through oral administration. The nano-micelles demonstrated improved dilution stability, enhanced greater mucosal adherence, significant P-gp efflux inhibition, and increased drug transport in the intestine by paracellular and transcellular pathways. Consequently, both the in vivo pharmacokinetic profile and therapeutic efficacy of SN38 against cancer were substantially improved via the micellar system. Thus, the developed polymeric micelles can potentially enhance the SN38 oral absorption for cancer therapy, offering prospective avenues for further exploration. • Novel chitosan derivative, N-Deoxycholic acid grafted N'-nonyl-trimethyl chitosan, enabled nano-micelle assembly. • Stable micelles loaded with SN38 were prepared for improving its oral delivery. • The micelles exhibited enhanced mucosal adhesion, P-gp inhibition, and intestinal drug transport. • Micellar system improved the oral bioavailability and anticancer efficacy of SN38. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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