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

Author:

Miraghaie Seyyed Hossein123,Zandi Ashkan24,Davari Zahra23,Mousavi‐kiasary Mohamad Sadegh2ORCID,Saghafi Zohre2,Gilani Ali2,Kordehlachin Yasin2,Shojaeian Fatemeh25,Mamdouh Amir2,Heydari Zahra6,Dorkoosh Farid Abedin3,Kaffashi Babak7,Abdolahad Mohammad238ORCID

Affiliation:

1. Department of Polymer Engineering Kish International Campus, University of Tehran Kish Island 79416‐55664 Iran

2. Nano Electronic Center of Excellence Nano‐bioelectronic Devices Lab., Cancer Electronics Research Group, School of Electrical and Computer Eng., College of Engineering, University of Tehran Tehran 14395–515 Iran

3. Department of Pharmaceutics Faculty of Pharmacy, Tehran University of Medical Sciences Tehran 14176‐14411 Iran

4. Nano Electronic Center of Excellence Nano‐electronics and Thin Film Lab., School of Electrical and Computer Eng., College of Engineering, University of Tehran Tehran 14395–515 Iran

5. School of Medicine Shahid Beheshti University of Medical Sciences Tehran 19615‐1179 Iran

6. Preclinical lab Core facility, Tehran University of Medical Sciences Tehran 14174‐66191 Iran

7. Department of Polymer Engineering School of Chemical Engineering, College of Engineering, University of Tehran Tehran 11155‐4563 Iran

8. Cancer Institute Tehran University of Medical Sciences Tehran 1416753955 Iran

Abstract

AbstractPure 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.

Funder

University of Tehran

Iran National Science Foundation

Publisher

Wiley

Subject

Materials Chemistry,Polymers and Plastics,Biomaterials,Bioengineering,Biotechnology

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