Design, Formulation and in vivo Evaluation of Novel Honokiol-Loaded PEGylated PLGA Nanocapsules for Treatment of Breast Cancer
Yusuf A Haggag,1 Rowida R Ibrahim,2 Amin A Hafiz3 1Department of Pharmaceutical Technology, Faculty of Pharmacy, Tanta University, Tanta, Egypt; 2Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Tanta University, Tanta, Egypt; 3Department of Clinical Nutrition, Faculty of...
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| Formato: | article |
| Lenguaje: | EN |
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Dove Medical Press
2020
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| Acceso en línea: | https://doaj.org/article/5bb6419a61d74e85ab1c8db9eb1b1da0 |
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| Sumario: | Yusuf A Haggag,1 Rowida R Ibrahim,2 Amin A Hafiz3 1Department of Pharmaceutical Technology, Faculty of Pharmacy, Tanta University, Tanta, Egypt; 2Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Tanta University, Tanta, Egypt; 3Department of Clinical Nutrition, Faculty of Applied Medical Sciences, Umm Al-Qura University, Mecca, Kingdom of Saudi ArabiaCorrespondence: Yusuf A HaggagDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Tanta University, Tanta 31111, EgyptTel +2 01220104612Fax +2 040 3335466Email youssif.hagag@pharm.tanta.edu.egBackground: Honokiol (HK) is a common herbal medicine extracted from magnolia plants. Low aqueous solubility and limited bioavailability of HK have hindered its clinical application, especially for cancer treatment. Nano-drug delivery system has the potential to enhance HK delivery and therefore, enhance its anti-cancer activity.Purpose: The study’s aim is to design novel PEGylated-PLGA polymeric nanocapsules (NCs) for HK delivery to breast tumor-bearing mice after systemic administration.Methods: Formulation of different HK-loaded NCs and their physio-chemical characterization were optimized through the use of different formulation variables. The antitumor activity of the HK-loaded NCs was investigated both in vitro using MCF-7 and EAC breast cancer cell lines and in vivo using solid Ehrlich carcinoma (SEC) breast cancer model.Results: The optimum HK-loaded NCs were prepared from 15% PEG-PLGA diblock copolymer and exhibited the lowest nano size of 125 nm, smooth spherical morphology, highest drug loading of 94% and highest cellular uptake into breast cancer cells. HK-loaded PEGylated NCs can effectively inhibit the in vitro cell growth of breast cancer cells by 80.2% and 58.1% compared to 35% and 31% with free HK in the case of MCF-7 and EAC, respectively. HK-loaded NCs inhibited SEC tumor growth by 2.3 fold significantly higher than free HK, in vivo.Conclusion: The designed drug delivery system encapsulating HK exhibited a pronounced decrease in tumor growth biomarkers meanwhile proved its safety in animals. Therefore, 15% PEGylated HK-loaded NCs may act as a promising new approach for breast cancer treatment.Keywords: honokiol, nanocapsule, PEG-PLGA copolymers, formulation variables, anti-cancer activity, solid Ehrlich carcinoma, breast cancer |
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