Thermosensitive Polymer-Modified Mesoporous Silica for pH and Temperature-Responsive Drug Delivery

Author:

Thirupathi Kokila1,Santhamoorthy Madhappan2,Radhakrishnan Sivaprakasam3,Ulagesan Selvakumari4ORCID,Nam Taek-Jeong5ORCID,Phan Thi Tuong Vy67ORCID,Kim Seong-Cheol2

Affiliation:

1. Department of Physics, Government Arts and Science College for Women, Karimangalam, Dharmapuri 635111, Tamil Nadu, India

2. School of Chemical Engineering, Yeungnam University, Gyeongsan 38541, Republic of Korea

3. Department of Organic Materials and Fiber Engineering, Jeonbuk National University, 567 Baekje-daero, Deokjin-gu, Jeonju-si 54896, Republic of Korea

4. Division of Fisheries Life Sciences, Pukyong National University, Nam-gu, Busan 48513, Republic of Korea

5. Institute of Fisheries Sciences, Pukyong National University, Gijang-gun, Busan 46041, Republic of Korea

6. Center for Advanced Chemistry, Institute of Research and Development, Duy Tan University, 03 Quang Trung, Hai Chau, Danang 550000, Vietnam

7. Faculty of Environmental and Chemical Engineering, Duy Tan University, 03 Quang Trung, Hai Chau, Danang 550000, Vietnam

Abstract

A mesoporous silica-based drug delivery system (MS@PNIPAm-PAAm NPs) was synthesized by conjugating the PNIPAm-PAAm copolymer onto the mesoporous silica (MS) surface as a gatekeeper that responds to temperature and pH changes. The drug delivery studies are carried out in vitro at different pH (7.4, 6.5, and 5.0) and temperatures (such as 25 °C and 42 °C, respectively). The surface conjugated copolymer (PNIPAm-PAAm) acts as a gatekeeper below the lower critical solution temperature (LCST) (<32 °C) and as a collapsed globule structure above LCST (>32 °C), resulting in controlled drug delivery from the MS@PNIPAm-PAAm system. Furthermore, the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and cellular internalization results support the prepared MS@PNIPAm-PAAm NPs being biocompatible and readily taken up by MDA-MB-231 cells. The prepared MS@PNIPAm-PAAm NPs, with their pH-responsive drug release behavior and good biocompatibility, could be used as a drug delivery vehicle where sustained drug release at higher temperatures is required.

Funder

National Research Foundation of Korea

Technology Development Program

Publisher

MDPI AG

Subject

Pharmaceutical Science

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