PH‐Triggered Sustained Drug Delivery from a Polymer Micelle having the β‐Thiopropionate Linkage. Issue 18 (22nd July 2016)

• Record Type: Journal Article
• Authors: Pramanik, Prithankar; Halder, Debdatta; Jana, Siddhartha Sankar; Ghosh, Suhrit
• Is Part Of: Macromolecular rapid communications. Volume 37:Issue 18(2016)
• Page Start: 1499
• Page End: 1506
• Publication Date: 2016-07-22
• Subjects: amphiphilic polymers -- β‐thiopropionate linkages -- doxorubicin -- drug delivery -- pH‐responsive micelles; Macromolecules -- Periodicals; Polymers -- Periodicals; Chemistry -- Periodicals; 547.705
• DOI: 10.1002/marc.201600260
• Languages: English
• ISSNs: 1022-1336

Abstract

Abstract : The synthesis, micellar aggregation, and pH‐triggered intracellular drug delivery ability of an amphiphilic statistical copolymer (P2) are studied. Two methacrylate derivatives, one containing a hydrophilic pendant and the other containing a hydrophobic pendant chain, are copolymerized to produce P2. The hydrophobic pendant chain is linked to the polymer backbone by a β‐thiopropionate linkage, known to undergo slow hydrolysis at mild acidic pH. P2 forms a multimicellar cluster in water with a critical aggregation concentration of 0.02 mg mL −1 and encapsulates a hydrophobic guest such as pyrene, Nile red, or the anti‐cancer drug doxorubicin (Dox). Sustained release of the entrapped Dox (80% after 100 h) is noticed at pH 5.2, while release is significantly slower (35% after 100 h) at pH 7.4. Acidic hydrolysis of the β‐thiopropionate linkage leading to the reduction of the hydrophobicity is established as the cause for micellar disassembly and triggered drug release. Cell‐culture studies with the human breast cancer cell line, MCF‐7, reveal biocompatibility of P2 (below 150 μg mL −1 ). It is further tested for intracellular delivery of Dox. MCF‐7 cells remain healthy at pH 7.4 but become unhealthy at pH 5.2 when treated with a Dox‐loaded P2 micelles. Abstract : An effective design for pH‐responsive polymeric micelle is demonstrated and utilized as a nanocontainer for intracellular sustained drug delivery in cancer cells. The strategy relies on slow hydrolysis of the as yet unexplored β‐thiopropionate linkage connecting the hydrophobic chains to the polymer backbone.