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Self-microemulsifying drug delivery system (SMEDDS) improves anticancer effect of oral 9-nitrocamptothecin on human cancer xenografts in nude mice

journal contribution
posted on 2024-11-01, 04:19 authored by Juan Li Lu, Jian Cheng Wang, Shu Xin Zhao, Xiao Yan Liu, Hui Zhao, Xuan Zhang, Shufeng Zhou, Qiang Zhang
9-Nitrocamptothecin (9-NC) is an orally administered topoisomerase-I inhibitor for the treatment of pancreatic carcinoma, but its oral absorption and bioavailability are poor. The main objective of this study was to develop optimal 9-nitrocamptothecin (9-NC) microemulsion prepared by self-microemulsifying drug delivery system (SMEDDS). Two SMEDDS formulations of 9-NC prepared from a mixture of ethyl oleate, Tween-80 (T-form) or Cremophor EL (C-form), and PEG-400/ethanol were formed as microemulsions under dilution with aqueous phase. The resulting microemulsions were evaluated in vitro and in vivo, including the kinetics and antitumor effects in SKOV-3 human ovarian cancer xenograft in nude mice. Following 1:10 aqueous dilution of optimal 9-NC SMEDDS, the droplet sizes of resulting microemulsions were (30.8 ± 4.6) nm and (39.8 ± 8.2) nm for SMEDDS T-form and C-form, respectively, and the zeta potential values were -(4.3 ± 0.5) mV and -(5.7 ± 0.5) mV, respectively. In SKOV-3 cells, the growth inhibition (IC50) of various 9-NC formulations was greatest with SMEDDS T-form (3.5 ± 0.7 nM) followed by SMEDDS C-form (4.6 ± 0.4 nM), 9-NC solution (6.6 ± 1.4 nM) and 9-NC suspension (26.0 ± 2.9 nM) (P < 0.01). It was indicated that the area under the plasma concentration¿time curve (AUC0?8 h) values of various formulations of 9-NC after oral administration ranked as the following sequence: SMEDDS T-form (360.12 ± 19.44 ng h/ml) -- SMEDDS C-form (351.71 ± 33.66 ng h/ml) > 9-NC solution (241.21 ± 24.67 ng h/ml) > 9-NC suspension (161.24 ± 24.31 ng h/ml). The 9-NC SMEDDS formulations also produced significantly more tumor shrinkage (P < 0.01) when compared to 9-NC suspension in nude mice bearing human ovarian cancer xenografts. The results suggest that SMEDDS is a promising drug delivery system to increase the oral bioavailability and antitumor effects of 9-NC and may be applied to other lipophilic drugs. 9-NC SMEDDS represents a novel 9-NC therapy for cancer patients.

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  1. 1.
    ISSN - Is published in 09396411

Journal

European Journal of Pharmaceutics and Biopharmaceutics

Volume

69

Issue

3

Start page

899

End page

907

Total pages

9

Publisher

Elsevier BV

Place published

Netherlands

Language

English

Copyright

Copyright © 2008 Elsevier B.V. All rights reserved.

Former Identifier

2006007930

Esploro creation date

2020-06-22

Fedora creation date

2009-08-03

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