| Literature DB >> 35450653 |
Thien Hoang Truong1, Khent Primo Alcantara1, Bryan Paul I Bulatao2, Feuangthit Niyamissara Sorasitthiyanukarn3, Chawanphat Muangnoi4, Nonthaneth Nalinratana5, Opa Vajragupta6, Pornchai Rojsitthisak7, Pranee Rojsitthisak8.
Abstract
Chitosan (Ch)-coated nanostructured lipid carriers (NLCs) have great potential for transdermal delivery with high localization of chemotherapeutics in breast cancer. This study used tetrahydrocurcumin (THC), a primary metabolite of curcumin with enhanced antioxidant and anticancer properties, as a model compound to prepare NLCs. Response surface methodology was employed to optimize THC-loaded Ch-coated NLCs (THC-Ch-NLCs) fabricated by high-shear homogenization. The optimized THC-Ch-NLCs had particle size of 244 ± 18 nm, zeta potential of -17.5 ± 0.5 mV, entrapment efficiency of 76.6 ± 0.2% and drug loading of 0.28 ± 0.01%. In vitro release study of THC-Ch-NLCs showed sustained release following the Korsmeyer-Peppas model with Fickian and non-Fickian diffusion at pH 7.4 and 5.5, respectively. THC-Ch-NLCs demonstrated significantly enhanced in vitro skin permeation, cell uptake, and remarkable cytotoxicity toward MD-MBA-231 breast cancer cells compared to the unencapsulated THC, suggesting Ch-NLCs as potential transdermal nanocarriers of THC for triple-negative breast cancer treatment.Entities:
Keywords: Breast cancer; Chitosan; Cytotoxicity; Nanostructured lipid carriers; Tetrahydrocurcumin; Transdermal delivery
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Year: 2022 PMID: 35450653 DOI: 10.1016/j.carbpol.2022.119401
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381