pH sensitive polyelectrolyte complex micelles for highly effective combination chemotherapy
- Authors
- Ramasamy, Thiruganesh; Kim, Jeong Hwan; Choi, Ju Yeon; Tuan Hiep Tran; Choi, Han-Gon; Yong, Chul Soon; Kim, Jong Oh
- Issue Date
- Jul-2014
- Publisher
- ROYAL SOC CHEMISTRY
- Keywords
- DRUG; NANOPARTICLES; THERAPY; PHARMACOKINETICS; ANTICANCER; DOXORUBICIN; BLOCK IONOMER COMPLEXES; CANCER; DELIVERY; PACLITAXEL
- Citation
- JOURNAL OF MATERIALS CHEMISTRY B, v.2, no.37, pp 6324 - 6333
- Pages
- 10
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- JOURNAL OF MATERIALS CHEMISTRY B
- Volume
- 2
- Number
- 37
- Start Page
- 6324
- End Page
- 6333
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/25906
- DOI
- 10.1039/c4tb00867g
- ISSN
- 2050-7518
2050-750X
- Abstract
- The co-encapsulation of two or more drugs in the same carrier affords synergistic therapeutic effects and enhanced therapeutic potency. For this, polyethylene oxide-b-polyacrylic acid di-block polymer based-smart pH-sensitive di-block polyelectrolyte complex (PEC) micelles were designed to encapsulate mitoxantrone (MTX) and doxorubicin (DOX) with high payload capacity and precise drug ratio. Three molar ratios (MTX/DOX: 2 : 1, 1 : 1, 1 : 2) of the drug-loaded PECs were prepared with high payload capacity and evaluated for various physicochemical characteristics. The dual drug combination exhibited a synergistic cytotoxic activity against both sensitive (MCF-7 and A-549) and resistant cancer cell lines (MDA-MB-231), unlike the individual drugs. Dual drug-loaded nanosystems (MTX/DOX-M) prolonged the blood circulation of drugs, and a synergic ratio was maintained throughout the study period. MTX/DOX-M exhibited superior therapeutic efficacy in xenograft models; by contrast, the free drug cocktail caused a significant loss of body weight in mice. Taken together, our results suggest that PEC micelles have great potential as nano-scaled therapeutic delivery systems for combination chemotherapy.
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