In-situ reaction compatibilization modification of poly(butylene succinate-co-terephthalate)/polylactide acid blend films by multifunctional epoxy compound.

Poly(butylene succinate-co-terephthalate) (PBST) copolyester, is a new type of biodegradable synthetic polymer material that has emerged in recent years, but it cannot meet the market requirements, because of its low strength. The high-strength and high-modulus polylactic acid (PLA) was blended with PBST to increase its strength, and the chain extender ADR-4370 was used to modify PBST/PLA films by reaction and compatibilization. Compared with the 80/20 wt% PBST/PLA films, the tensile strength after modification with 0.3 wt% ADR was increased by 21.8 % and 44.3 % in the machine direction (MD) and in the transverse direction (TD), respectively. The Water Vapor Permeability (WVP) was decreased from 10.0 × 10-14 to 3.09 × 10-14 g·cm/cm2·s·Pa. The compatibilization mechanism was studied by gel permeation chromatography, infrared spectroscopy, dynamic mechanical analysis, rheological analysis, and other characterization methods. The formation of the copolymer PLA-g-PBST is the most important factor to improve the compatibility of the system and the mechanical properties of the films.

Poly (lactic acid) blends with excellent low temperature toughness: A comparative study on poly (lactic acid) blends with different toughening agents.

Poly (lactic acid) (PLA) blends with different toughening agents were prepared by melt compounding, and the effects of toughening agents on the toughness of PLA, especially the low-temperature toughness, were investigated. All blends were immiscible systems, but the rheological Cole-Cole diagram showed that the blends had certain compatibility, and the interfacial bonding of PLA/Ethylene/butyl methacrylate/Glycidyl Methacrylate Terpolymer (GEBMA) blend was the best. With addition of the toughening agents, all blends showed improvement of the tensile and impact toughness both at room temperature and low temperature. GEBMA was the best toughening agent, the elongation at break and impact strength at room temperature and low temperature were greatly improved. The elongation at break, tensile strength and impact strength of PLA blend with 20 wt% GEBMA at -20 °C was 55.8 MPa, 195.9% and 18.8 kJ/m2, respectively, which showed the reinforcement and super ductility at low temperature. However, the toughening effect of Poly (propylene carbonate) polyurethane (PPCU) at low temperature was poor. The Tg and interfacial bonding were the main factors affecting the toughness of the blends, especially at low temperature. The lower the Tg and the better the interfacial bonding, the better the toughness of the blends.

Preparation and properties of poly(L-lactic acid) blends with excellent low-temperature toughness by blending acrylic ester based impact resistance agent.

Poly(L-lactic acid) (PLLA) blends with excellent low-temperature toughness and strength were prepared by melt compounding with acrylic ester based impact resistance agent (AEIR). The morphology, thermal properties, mechanical properties and biodegradability of the blends were investigated. Morphology observations revealed the blend was immiscible but had good compatibility with the dispersed phase size of about 200-300 nm. With the addition of AEIR, dramatic improvement in toughness of PLLA was achieved in a wide temperature range, especially at low temperatures the tensile strength was effectively remained. For the blend with 20 wt% AEIR, the tensile strength, elongation at break and impact strength were 51.6 MPa, 72% and 77.1 KJ/m2 at -20 °C, respectively, much greater than that reported. The calculated Tg of AEIR was lower than the test temperatures, and the brittle-tough transition occurred. The PLLA matrix demonstrated obvious shear yielding which induced energy dissipation and therefore lead to excellent toughness of the blends. Moreover, the biodegradation of PLLA was enhanced after blends preparation.

Fiber-induced crystallization in polymer composites: A comparative study on poly(lactic acid) composites filled with basalt fiber and fiber powder.

The poly(lactic acid) (PLA) composites with the silane coupling agent treated basalt fiber (SBF) and basalt fiber powder (SBFP) were prepared. The crystalline morphology, mechanical properties, and heat resistance of PLA/SBF/SBFP composites were investigated. The results indicated that SBF or SBFP not only acted as heterogeneous nucleating agents for PLA crystallization but also improved the mechanical properties and heat resistance of PLA. Morphological analyses showed that SBFP could play nucleating role to reduce the spherulites size of PLA, and SBF could restrict the mobility of PLA chains and construct interface crystallization for PLA during isothermal crystallization process. The composites with higher SBF loading, the "Transcrystalline-network" built in the composites significantly improved the heat resistance properties of PLA. Due to the synergistic effect of SBF and SBFP, the PLA/SBF/SBFP composites showed high heat deformation temperature (HDT), especially after isothermal crystallization, the HDT increased to 150.5 °C for the PLA/SBF/SBFP 50/10/40 composite, much higher (about 190%) than that of pure PLA (71.7 °C).

LC-MS/MS assay for the determination of tat-K13, a novel interfering peptide for the treatment of ischemic stroke, in human plasma and its application to a pharmacokinetics study.

A sensitive and robust method has been developed using an ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) assay to quantify Tat-K13, a novel interfering peptide for the treatment of ischemic stroke, in human plasma. Automated solid-phase extraction on a Waters Oasis WCX (30 µm, 10 mg) 96-well plate was used to extract Tat-K13 from human plasma and the extracts were separated on a Waters Acquity CSH column (2.1 × 50 mm i.d., 1.7 µm) with a gradient elution method by mobile phase A (nonafluoropentanoic acid-acetic acid-water, 1:2:1000, v/v/v) and B (nonafluoropentanoic acid-acetic acid-water-acetonitrile, 1:2:100:900, v/v/v/v). The method was fully validated following international bioanalytical guidelines and showed good linearity from 2.10 to 1,050 ng/ml. The method was successfully applied to investigate the clinical pharmacokinetics of Tat-K13 in health volunteers. Rapid elimination of Tat-K13 from the body was observed, with half-life ranging from 0.26 to 0.78 h across different dose levels. The exposure of Tat-K13 was approximately dose-dependent in terms of the area under the concentration-time curve and peak concentration.

Effect of molecular stereoregularity on the transcrystallinization properties of poly(l-lactide)/basalt fiber composites.

A comparative study on interfacial crystallization of poly(l-lactic acid) (PLLA) with different stereoregularity (PLLA2003D 96.0%, PLLA4032D 98.5%, and PLLA290 99.2%) surrounding macroscopic basalt fibers (BF) has been carried out in polymer composites. The effect of stereoregularity on the interface crystallization was systemically studied by microstructure. From polarized optical microscopy (POM) analysis, it was found that the transcrystallinity of PLLA was influenced by temperature. Moreover, stereoregularity significantly affects the crystallization kinetics. It was also found that increased molecular mobility providing faster orientation with high stereoregularity and low molecular weight. It might be the reason for the observation that the PLLA290 samples crystallized more rapidly than the PLLA4032D samples. Appropriate molecular stereoregularity exhibits a clear increase in extensional stress that is directly correlated with the crystalline orientation of the crystallization samples. The mechanism of formation of transcrystallinity underwent the process of "a mismatch in thermal expansion coefficients" with the extensional stress.

Effect of Ethylene/butyl methacrylate/Glycidyl Methacrylate Terpolymer on toughness and biodegradation of poly (l-lactic acid).

The super toughed poly(l-lactic acid) (PLLA) blends with various content of Ethylene/butyl methacrylate/Glycidyl Methacrylate Terpolymer (GEBMA) were prepared by melt compounding. The blend was an immiscible system but had good compatibility due to the chemical reaction between the epoxy groups of GEBMA and the end group of PLLA during the blending process. The addition of GEBMA suppressed the cold crystallization and non-isothermal melt crystallization of PLLA. GEBMA was a very effective toughening agent for PLLA. The addition of only 15 wt% GEBMA, the elongation at break and impact strength of the blend were significantly improved compared to neat PLLA, which were 63 and 18 times that of neat PLLA, respectively. Scanning electron microscopy (SEM) images of the impact fracture surfaces of the blends showed a large amount of cavities and plastic deformation in the blend, which induced energy dissipation and therefore led to the improvement in toughness of the PLLA/GEBMA blends. For the PLLA/GEBMA blown films, the addition of GEBMA significantly improved the flexibility of PLLA/GEBMA blown film. The tear strength reached a maximum of 143.5 kN/m in the machine direction (MD) and 166.7 kN/m in the transverse direction (TD). Moreover, the biodegradation of PLLA was enhanced after blends preparation.

Exploring polylactide/poly(butylene adipate-co-terephthalate)/rare earth complexes biodegradable light conversion agricultural films.

In this work, rare earth europium was combined with different organic ligands to obtain two kinds of rare earth conversion agents, Eu(DBM)4CPC and Eu(TTA)3(TPPO)2. Two kinds of conversion films were successfully prepared by combining them with polylactide and poly(butylene adipate-co-terephthalate). Results showed that the film has excellent light conversion ability and high color purity, and rare earth complexes improved melt flowing property and decreased melt viscosity of blend. At the same time, the elongation at break of the film increased greatly, which could up to 595.0/460.9% in the both machine direction (MD) and transverse direction (TD). The results of GPC show that rare earth complexes can make main chain of PLA scission, which causes rapid molecular weight reduction, and the effect of Eu(DBM)4CPC on the molecular weight of PLA was more significant than Eu(TTA)3(TPPO)2. SEM shows that the complicity of PLA and PBAT has been improved, the dispersed phase of the blend is more uniform. DSC shows that both rare earth complexes can improve the crystallization capacity of PLA. And with the addition of cetylpyridinium chloride could improve the compatibility of rare earth complexes and polymer materials, the light transmittance and hydrophilicity of the film also increased obviously.

Neuroactive Steroids. 1. Positive Allosteric Modulators of the (γ-Aminobutyric Acid)A Receptor: Structure-Activity Relationships of Heterocyclic Substitution at C-21.

Neuroactive steroids (NASs) have been shown to impact central nervous system (CNS) function through positive allosteric modulation of the GABA(A) receptor (GABA(A)-R). Herein we report the effects on the activity and pharmacokinetic properties of a series of nor-19 pregnanolone analogues bearing a heterocyclic substituent at C-21. These efforts resulted in the identification of SGE-516, a balanced synaptic/extrasynaptic GABA(A) receptor modulator, and SGE-872, a selective extrasynaptic GABA(A) receptor modulator. Both molecules possess excellent druglike properties, making them advanced leads for oral delivery of GABA(A) receptor modulators.