TY - JOUR
T1 - Biodegradable Poly(Acetonide Gluconic Acid) for Controlled Drug Delivery
AU - Abtew, Ester
AU - Ezra, Aviva F.
AU - Basu, Arijit
AU - Domb, Abraham J.
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/8/12
Y1 - 2019/8/12
N2 - We report here on the synthesis, characterization, degradation, and drug release of acetal-protected gluconic acid-based poly(α-hydroxy ester). This polyester was synthesized by ring-opening polymerization of O-carboxyanhydride of acetal-protected gluconic acid. The polymer undergoes hydrolytic degradation under mild acidic media, whereas minimal degradation takes place under physiological pH. Under acidic conditions, the acetal-protecting groups are hydrolyzed, resulting in a water-soluble polyester with saccharide side chains that erodes from the surface, leaving the bulk of the polymer matrix intact. At pH 3.5, zero-order kinetics was maintained for 50 days accounting for ∼75% drug release. These biodegradable, pH-responsive, sustained zero-order release kinetics of the polymer have application as drug carriers for oral drug delivery or medical implants or also for nonmedical applications.
AB - We report here on the synthesis, characterization, degradation, and drug release of acetal-protected gluconic acid-based poly(α-hydroxy ester). This polyester was synthesized by ring-opening polymerization of O-carboxyanhydride of acetal-protected gluconic acid. The polymer undergoes hydrolytic degradation under mild acidic media, whereas minimal degradation takes place under physiological pH. Under acidic conditions, the acetal-protecting groups are hydrolyzed, resulting in a water-soluble polyester with saccharide side chains that erodes from the surface, leaving the bulk of the polymer matrix intact. At pH 3.5, zero-order kinetics was maintained for 50 days accounting for ∼75% drug release. These biodegradable, pH-responsive, sustained zero-order release kinetics of the polymer have application as drug carriers for oral drug delivery or medical implants or also for nonmedical applications.
UR - http://www.scopus.com/inward/record.url?scp=85071287189&partnerID=8YFLogxK
U2 - 10.1021/acs.biomac.9b00461
DO - 10.1021/acs.biomac.9b00461
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C2 - 31259534
AN - SCOPUS:85071287189
SN - 1525-7797
VL - 20
SP - 2934
EP - 2941
JO - Biomacromolecules
JF - Biomacromolecules
IS - 8
ER -