Targeted Delivery of Anticancer Drug Loaded Charged PLGA Polymeric Nanoparticles Using Electrostatic Field

被引:2
作者
Miraghaie, Seyyed Hossein [1 ,2 ,3 ]
Zandi, Ashkan [2 ,4 ]
Davari, Zahra [2 ,3 ]
Mousavi-kiasary, Mohamad Sadegh [2 ]
Saghafi, Zohre [2 ]
Gilani, Ali [2 ]
Kordehlachin, Yasin [2 ]
Shojaeian, Fatemeh [2 ,5 ]
Mamdouh, Amir [2 ]
Heydari, Zahra [6 ]
Dorkoosh, Farid Abedin [3 ]
Kaffashi, Babak [7 ]
Abdolahad, Mohammad [2 ,3 ,8 ]
机构
[1] Univ Tehran, Dept Polymer Engn, Kish Int Campus, Kish 7941655664, Iran
[2] Univ Tehran, Coll Engn, Nano Elect Ctr Excellence, Sch Elect & Comp Eng,Canc Elect Res Grp,Nanobioele, Tehran 14395515, Iran
[3] Univ Tehran Med Sci, Fac Pharm, Dept Pharmaceut, Tehran 1417614411, Iran
[4] Univ Tehran, Coll Engn, Nano Elect Ctr Excellence, Sch Elect & Comp Eng,Nanoelect & Thin Film Lab, Tehran 14395515, Iran
[5] Shahid Beheshti Univ Med Sci, Sch Med, Tehran 196151179, Iran
[6] Univ Tehran Med Sci, Preclin Lab, Core Facil, Tehran 1417466191, Iran
[7] Univ Tehran, Coll Engn, Sch Chem Engn, Dept Polymer Engn, Tehran 111554563, Iran
[8] Univ Tehran Med Sci, Canc Inst, Tehran 1416753955, Iran
关键词
animal study; cancer; charged polymeric nano-particles; electrostatic field; optimized chemotherapy; targeted drug delivery; IN-VITRO; PACLITAXEL; THERAPY; MICROSPHERES; PERMEABILITY; ACID;
D O I
10.1002/mabi.202300181
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pure positive electrostatic charges (PPECs) show suppressive effect on the proliferation and metabolism of invasive cancer cells without affecting normal tissues. PPECs are used for the delivery of drug-loaded polymeric nanoparticles (DLNs) capped with negatively charged poly(lactide-co-glycolide) (PLGA) and Poly(vinyl-alcohol) PVA into the tumor site of mouse models. The charged patch is installed on top of the skin in the mouse models' tumor region, and the controlled selective release of the drug is assayed by biochemical, radiological, and histological experiments on both tumorized models and normal rats' livers. It is found that DLNs synthesized by PLGA show great attraction to PPECs due to their stable negative charges, which would not degrade immediately in blood. The burst and drug release after less than 48h of this synthesized DLNs are 10% and 50%, respectively. These compounds can deliver the loaded-drug into the tumor site with the assistance of PPECs, and the targeted-retarded release will take place. Hence, local therapy can be achieved with much lower drug concentration (conventional chemotherapy [2 mg kg(-1)] versus DLNs-based chemotherapy [0.75 mg kg(-1)]) with negligible side effects in non-targeted organs. PPECs have many potential clinical applications for advanced-targeted chemotherapy with the lowest discernible side effects.
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页数:15
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