Design, development and evaluation of Resveratrol transdermal patches for breast cancer therapy

被引:8
|
作者
Gadag, Shivaprasad [1 ]
Narayan, Reema [1 ]
Nayak, Yogendra [2 ]
Garg, Sanjay [3 ]
Nayak, Usha Y. [1 ]
机构
[1] Manipal Acad Higher Educ, Manipal Coll Pharmaceut Sci, Dept Pharmaceut, Manipal 576104, Karnataka, India
[2] Manipal Acad Higher Educ, Manipal Coll Pharmaceut Sci, Dept Pharmacol, Manipal 576104, Karnataka, India
[3] Univ South Australia, UniSA Clin & Hlth Sci, Adelaide, SA 5000, Australia
关键词
Breast cancer; Flux; Localized delivery; QSPR; Resveratrol; Transdermal patch; SOLID LIPID NANOPARTICLES; IN-VITRO; TRANS-RESVERATROL; DELIVERY; PHARMACOKINETICS;
D O I
10.1016/j.ijpharm.2022.122558
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Resveratrol (RVT) is a polyphenolic phytoestrogen which has shown antiproliferative activity in breast cancer. However, its low bioavailability and short half-life have restricted its use. The current study aimed to develop transdermal patches of RVT and evaluate its site-specific delivery for breast cancer therapy. Different penetration enhancers were screened using a computational tool, quantitative structure propery relationship (QSPR). The best permeation of RVT was observed in a patch comprising hydroxypropyl methylcellulose (HPMC) E15LV: HPMC-K4M: polyvinyl pyrrolidone (PVP) K30 in the ratio of 3:1:2 as release controlling polymers with Glycerol: Capryol 90 (4:1) as penetration enhancer and plasticizer. To assess the localized delivery of RVT, the patch was applied to the breast of female rats. Higher breast tissue disposition with lower systemic concentration was observed compared to oral administration, demonstrated by increased AUC and MRT. Further, the optimized RVT patches were tested in 7,12-Dimethylbenz[a]anthracene (DMBA) induced rat mammary cancer. Compared to oral RVT, the application of RVT tansdermal patches significantly reduced the tumor volume and serum CA 15-3, a cancer biomarker. Thus, the RVT transdermal patch may be a viable approach for ensuring high local concentration of drug for site-specific delivery in breast cancer therapy.
引用
收藏
页数:14
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