Stereocomplex Prodrugs of Oligo(lactic acid) -Gemcitabine in Poly(ethylene glycol)- block-poly(d,l-lactic acid) Micelles for Improved Physical Stability and Enhanced Antitumor Efficacy.

Herein we demonstrate the formation of stereocomplex prodrugs of oligo(l-lactic acid) -gemcitabine (o(LLA) -GEM) and oligo(d-lactic acid) -gemcitabine (o(DLA) -GEM) for stable incorporation in poly(ethylene glycol)- block-poly(d,l-lactic acid) (PEG- b-PLA) micelles. O(LLA) or o(DLA) was attached at the amino group (4-( N)) of GEM via an amide linkage. When n = 10, a 1:1 mixture of o(LLA)-GEM and o(DLA)-GEM (o(L+DLA)-GEM) was able to form a stereocomplex with a distinctive crystalline pattern. Degradation of o(L+DLA)-GEM was driven by both backbiting conversion and esterase contribution, generating primarily o(L+DLA)-GEM and GEM. O(L+DLA)-GEM stably loaded in PEG- b-PLA micelles in the size range of 140-200 nm with an unexpected elongated morphology. The resulting micelles showed improved physical stability in aqueous media and inhibited backbiting conversion of o(L+DLA)-GEM within micelles. Release of o(L+DLA)-GEM from micelles was relatively slow, with a t at ca. 60 h. Furthermore, weekly administration of o(L+DLA)-GEM micelles i.v. displayed potent antitumor activity in an A549 human non-small-cell lung carcinoma xenograft model. Thus, stereocomplexation of isotactic o(LLA) and o(DLA) acts as a potential prodrug strategy for improved stability and sustained drug release in PEG- b-PLA micelles.