Liquid crystalline assembly for potential combinatorial chemo-herbal drug delivery to lung cancer cells

被引:66
作者
Abdelaziz, Hadeer M. [1 ,2 ]
Elzoghby, Ahmed O. [1 ,3 ,4 ,5 ]
Helmy, Maged W. [1 ,6 ]
Samaha, Magda W. [1 ,3 ]
Fang, Jia-You [7 ,8 ,9 ,10 ]
Freag, May S. [1 ,4 ,5 ,11 ]
机构
[1] Alexandria Univ, Fac Pharm, CNRL, Alexandria 21521, Egypt
[2] Damanhur Univ, Dept Pharmaceut, Fac Pharm, Damanhur, Egypt
[3] Alexandria Univ, Dept Ind Pharm, Fac Pharm, Alexandria 21521, Egypt
[4] Harvard Med Sch, Brigham & Womens Hosp, Div Engn Med, Dept Med, Boston, MA 02115 USA
[5] Harvard MIT Div Hlth Sci & Technol HST, Cambridge, MA 02139 USA
[6] Damanhur Univ, Dept Pharmacol & Toxicol, Fac Pharm, Damanhur, Egypt
[7] Chang Gung Univ, Grad Inst Nat Prod, Pharmaceut Lab, Taoyuan 333, Taiwan
[8] Chang Gung Univ Sci & Technol, Res Ctr Ind Human Ecol, Taoyuan 333, Taiwan
[9] Chang Gung Univ Sci & Technol, Res Ctr Chinese Herbal Med, Taoyuan 333, Taiwan
[10] Chang Gung Mem Hosp, Dept Anesthesiol, Taoyuan 333, Taiwan
[11] Alexandria Univ, Dept Pharmaceut, Fac Pharm, 1 Azarita Sq, Alexandria 21521, Egypt
关键词
hydrophobic ion pairing; liquid crystalline nanoparticles; lung cancer; glyceryl monoolein; pemetrexed; resveratrol; TRANS-RESVERATROL; HPLC METHOD; VALIDATION;
D O I
10.2147/IJN.S188335
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: Lung cancer is the most common cancer and the leading cause of total deaths worldwide. Its classified into two major types including non-small cell lung carcinoma (NSCLC) and small cell lung carcinoma (SCLC) based on the origin of abnormal lung cells as well as the smoking status of the patient. NSCLC is the most common and aggressive type of lung cancer representing 80%-85% of all cases. Purpose: The aim of the study was to present lyotropic liquid crystalline nanoparticles (LCNPs) as promising carriers for co-delivery of the chemotherapeutic agent, pemetrexed (PMX) and the herbal drug, resveratrol (RSV) for effective lung cancer management. Methods: The proposed PMX-RSV-LCNPs were prepared by hydrotrope method. Hydrophobic ion pairing with cetyl trimethyl ammonium bromide (CTAB) was implemented to increase the encapsulation efficiency of the hydrophilic PMX up to 95%+/- 3.01%. Results: The tailored PMX-RSV-LCNPs exhibited a particle size of 173 +/- 0.26 nm and biphasic release pattern with a relatively initial burst release within first 3-4 hour followed by sustained release up to 24 hours. Moreover, PMX-RSV-LCNPs manifested superior concentration and time dependent cytotoxicity profile against A549 lung cancer cells with IC50 4.0628 mu g/mL. Besides, the enhanced cellular uptake profile based on bioadhesive properties of glyceryl monoolein (GMO) as well as energy independent (cholesterol dependent) pattern. In-vivo evaluations against urethane induced lung cancer bearing mice demonstrated the potentiality of PMX-RSV-LCNPs in tumor growth inhibition via inhibition of angiogenesis and induction of apoptosis. The results were supported by histopathological analysis and immunohistochemical Ki67 staining. Moreover, PMX-RSV-LCNPs displayed a promising safety profile via attenuating nephro- and hepatotoxicity. Conclusion: PMX-RSV-LCNPs elaborated in the current study hold a great promise for lung cancer treatment.
引用
收藏
页码:499 / 517
页数:19
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