| Literature DB >> 26412423 |
Chuan Li1, Jia Zhang2, Yu-Jiao Zu2, Shu-Fang Nie3, Jun Cao1, Qian Wang4, Shao-Ping Nie5, Ze-Yuan Deng5, Ming-Yong Xie5, Shu Wang6.
Abstract
Many phytochemicals show promise in cancer prevention and treatment, but their low aqueous solubility, poor stability, unfavorable bioavailability, and low target specificity make administering them at therapeutic doses unrealistic. This is particularly true for (-)-epigallocatechin gallate, curcumin, quercetin, resveratrol, and genistein. There is an increasing interest in developing novel delivery strategies for these natural products. Liposomes, micelles, nanoemulsions, solid lipid nanoparticles, nanostructured lipid carriers and poly (lactide-co-glycolide) nanoparticles are biocompatible and biodegradable nanoparticles. Those nanoparticles can increase the stability and solubility of phytochemicals, exhibit a sustained release property, enhance their absorption and bioavailability, protect them from premature enzymatic degradation or metabolism, prolong their circulation time, improve their target specificity to cancer cells or tumors via passive or targeted delivery, lower toxicity or side-effects to normal cells or tissues through preventing them from prematurely interacting with the biological environment, and enhance anti-cancer activities. Nanotechnology opens a door for developing phytochemical-loaded nanoparticles for prevention and treatment of cancer.Entities:
Keywords: (−)-Epigallocatechin Gallate; Biocompatible; Biodegradable; Cancer; Curcumin; Genistein; Nanoparticles; Quercetin; Resveratrol
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Year: 2015 PMID: 26412423 PMCID: PMC5488276 DOI: 10.1016/S1875-5364(15)30061-3
Source DB: PubMed Journal: Chin J Nat Med ISSN: 1875-5364