Polyanhydrides have been synthesized for decades by melt-polycondensation of diacid monomers and 5 to >10 times mole excess acetic anhydride to diacid monomers to form polymers with a polydispersity ranging from 2.5 to 6 and low reproducibility. Hydrophobic segments in polyanhydrides are beneficial to hinder the characteristic hydrolytic cleavage of an anhydride bond that provides stable polyanhydrides at room temperature. The objective of this work is to synthesize aliphatic polyanhydrides with various hydrophobic segments, controllable and reproducible molecular weight, and low polydispersity that are essential for potential use as drug carriers. A series of polyanhydrides of suberic, azelaic, sebacic, and dodecanedioic acids with controlled molecular weight, reduced polydispersity, and standard deviation of molecular weights, have been synthesized. All synthesized polyanhydrides were thoroughly characterized by NMR, Fourier transform infrared spectroscopy, and gel permeation chromatography. Molecular weights of the synthesized polyanhydrides are highly controllable, depending on the degree of activation of the dicarboxylic acid monomers, i.e., the amount of acetic anhydride used during synthesis. Polyanhydrides have been synthesized in triplicate by melt-polycondensation, using various mole ratios of acetic anhydride to diacids. The standard deviation of the molecular weights of the polyanhydrides is minute when using 1 equivalent of acetic anhydride during the activation of dicarboxylic acids, whereas if excess acetic anhydride is used, the standard deviation is very high. The effect of safe and natural inorganic catalysts, Calcium oxide, Zinc oxide, and Calcium carbonate on polymerization is also studied. As-synthesized poly(sebacic acid) can offer convenience to use in controlled drug delivery applications. In vitro drug release study using Temozolamide (TMZ), a medication used to treat brain tumors such as glioblastoma and anaplastic astrocytoma, shows 14% TMZ release after the first hour and 70% release over one day from the poly(sebacic acid) wafers.

We report on the synthesis of a series of poly(ester-anhydride) composed of the following dicarboxylic acids: adipic, suberic, sebacic, dodecanedioic acids; and hydroxyalkanoic acids: ricinoleic and 12-hydroxystearic acid with control molecular weight approaching from a new method in which well-defined ester monomers are first synthesized by stepwise addition of hydroxyalkanoic acids molecules into melted dicarboxylic acids. The key advantage of the synthesis of ester monomers in this modified method is the full consumption of hydroxy acid devoid of any self-condensation. The ester monomers are then activated using variable amounts of acetic anhydride followed by melt condensation polymerization. The molecular weights of the synthesized poly(ester-anhydride) are highly controllable depending upon the degree of activation of the ester monomers; hence the amount of acetic anhydride. All the synthesized poly(ester-anhydrides) are thoroughly characterized by 1 H NMR, Fourier transform infrared, and gel permeation chromatography.