Green self-assembled lactoferrin carboxymethyl cellulose nanogels for synergistic chemo/herbal breast cancer therapy

被引:27
作者
Atallah, Mai A. [1 ,2 ]
Sallam, Marwa A. [2 ]
Abdelmoneem, Mona A. [1 ,3 ]
Teleb, Mohamed [1 ,4 ]
Elkhodairy, Kadria A. [1 ,2 ]
Bekhit, Adnan A. [1 ,4 ,5 ]
Khafaga, Asmaa F. [6 ]
Noreldin, Ahmed E. [7 ]
Elzoghby, Ahmed O. [1 ,2 ]
Khattab, Sherine N. [1 ,8 ]
机构
[1] Alexandria Univ, Fac Pharm, Canc Nanotechnol Res Lab CNRL, Alexandria 21521, Egypt
[2] Alexandria Univ, Fac Pharm, Dept Ind Pharm, Alexandria 21521, Egypt
[3] Damanhur Univ, Fac Pharm, Dept Pharmaceut, Damanhur, Egypt
[4] Alexandria Univ, Fac Pharm, Dept Pharmaceut Chem, Alexandria 21521, Egypt
[5] Univ Bahrain, Coll Hlth & Sport Sci, Allied Hlth Dept, Pharm Program, POB 32038, Zallaq, Bahrain
[6] Alexandria Univ, Fac Vet Med, Dept Pathol, Edfina, Egypt
[7] Damanhur Univ, Fac Vet Med, Dept Histol & Cytol, Damanhur, Egypt
[8] Alexandria Univ, Fac Sci, Chem Dept, Alexandria 21321, Egypt
关键词
Lactoferrin; Carboxymethyl cellulose; Pemetrexed; Honokiol; Hydroxypropyl ?-cyclodextrin inclusion; complex; ETHYL 2-CYANO-2-(HYDROXYIMINO)ACETATE OXYMA; PHYSICOCHEMICAL CHARACTERIZATION; REPLACE; 1-HYDROXYBENZOTRIAZOLE; POLYELECTROLYTE COMPLEX; CONTROLLED-RELEASE; CASEIN MICELLES; IN-VITRO; DRUG; HONOKIOL; DELIVERY;
D O I
10.1016/j.colsurfb.2022.112657
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The current treatment protocols for breast cancer have shifted from single agent therapies to combinatorial approaches that offer synergistic efficacies and reduced side effects. Self-assembled nanogels comprising natural polysaccharides and functional proteins provide an intelligent platform for the targeted co-delivery of therapeutic molecules. Herein, we report the fabrication of self-assembled nanogels utilizing hydrophilic biocompatible proteins, lactoferrin (Lf), and polysaccharide carboxy methyl cellulose (CMC), for the combined delivery of the antimetabolite pemetrexed (PMT) and the herbal polyphenol honokiol (HK). PMT was conjugated to LF via an amide bond. The conjugate was then electrostatically assembled into CMC under optimized conditions to form nanogels (Lf-CMC NGs). An inclusion complex of HK with hydroxypropyl-beta-cyclodextrin was then encapsulated in the prepared Lf-CMC NGs with an entrapment efficiency of 66.67%. The dual drug-loaded cross-linked Lf-CMC NGs exhibited a particle size of 193.4 nm and zeta potential of - 34.5 mV and showed a sustained release profile for both drugs. PMT/HK-loaded Lf-CMC NGs were successfully taken up by MDA-MB-231 breast cancer cells and demonstrated superior in vitro cytotoxicity, as elucidated by a low combination index value (CI=0.17) and a higher dose reduction index (DRI) compared to those of the free drugs. An in vivo antitumor study using an Ehrlich ascites tumor (EAT) mouse model revealed the robust efficacy of PMT/HK-loaded Lf-CMC NGs in inhibiting tumor growth, which was ascribed to the reduced expression level of VEGF-1, elevated protein expression level of caspase-3, and suppressed Ki-67 protein level in the tumor tissue (P <0.05). In conclusion, our green fabricated self-assembled dual-loaded nanogels offer a promising biocompatible strategy for targeted combinatorial breast cancer therapy.
引用
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页数:15
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