Hydrolytic degradation linear

Commercial condensed phosphoric acids are mixtures of linear polyphosphoric acids made by the thermal process either direcdy or as a by-product of heat recovery. Wet-process acid may also be concentrated to - 70% P2O5 by evaporation. Liaear phosphoric acids are strongly hygroscopic and undergo viscosity changes and hydrolysis to less complex forms when exposed to moist air. Upon dissolution ia excess water, hydrolytic degradation to phosphoric acid occurs the hydrolysis rate is highly temperature-dependent. At 25°C, the half-life for the formation of phosphoric acid from the condensed forms is several days, whereas at 100°C the half-life is a matter of minutes. 

Hammer and coworkers prepared PEG-h-PCL polymersomes entrapping DXR (Fig. 11a). The release of DXR from the polymersomes was in a sustained manner over 14 days at 37 °C in PBS via drug permeation through the PCL membrane, and hydrolytic degradation of the PCL membrane [228]. The release rate of encapsulated molecules from polymersomes can be tuned by blending with another type of block copolymer [229]. Indeed, the release rate of encapsulated DXR from polymersomes prepared from mixtures of PEG- -PLA with PEG- -PBD copolymers increased linearly with the molar ratio of PEG- -PLA in acidic media (Fig. lib). Under acidic conditions, the PLA first underwent hydrolysis and, hours later, pores formed in the membrane followed by final membrane... 

The authors determined specificity using the known hydrolytic degradation products. The precision of spiked samples of these degradation products were determined and found to be acceptable (99.9 0.4%). Accuracy of the method was determined using spiked recoveries of piroxicam benzoate, and the recoveries were acceptable (99.1-100.5%). Assay precision n = 6, RSD = 0.4%) was in accord with recommended criteria [7]. Within-day precision was performed on two instruments on two separate days, and the overall intermediate precision was 1.0%. The method was linear over the expected analyte concentration range giving a regression line of 1 = 0.999. The detection (DL) and quantification levels (QL) were assessed, and the latter was determined as 0.185 pg/ml (ca. 0.04%). 

Galbis et al. described a variety of carbohydrate-based linear polyesters 61 of the poly(alkylene dicarboxylate) type that were obtained by polycondensation reactions of the alditols 2,3,4-tri-(9-methyl-L-arabinitol (9) and 2,3,4-tri-O-methyl-xylitol (10), and the aldaric acids 2,3,4-tri-(9-methyl-L-arabinaric acid (26) and 2,3,4-tri-(9-methyl-xylaric acid (27), butanediol, and adipic acid were also used as comonomers [28]. Copolyesters of the poly(aIkylene-c )-arylene dicarboxylate) type were obtained using bisphenols as comonomers (Scheme 1). Chemical polycondensation reactions were conducted in bulk or in solution. Enzymatic polycondensation reactions of adipic acid with the above-mentioned alditols were carried out successfully using Lipozyme and Novozyme 435. The hydrolytic degradations of some of these polyesters were also described. 

Schoonover, J. R., Thompson, D. G, et al. (2001), Infrared linear dichroism study of a hydrolytically degraded poly(ester Urethane). Polymer Degradation and Stability, 74, 87-96. 

Figure 15. SEM micrograph (3 5OX) of linear (top) and star-shaped (bottom) PGCL fibres after hydrolytic degradation for 2, 3,4, and 6 weeks, respectively.

Lindstrom and co-workers [4] carried out quantitative determinations of aqueous hydrolytic degradation prodncts prodnced in the early stages of degradation in linear and branched polybutylene adipate (PBA) and polybntylene succinate (PBS). 

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