Chitosan/calcium–alginate beads for oral delivery of insulin

A mild chitosan/calcium alginate microencapsulation process, as applied to encapsulation of biological macromolecules such as albumin and insulin, was investigated. The microcapsules were derived by adding dropwise a protein-containing sodium alginate mixture into a chitosan–CaCl₂ system. The beads containing a high concentration of entrapped bovine serum albumin (BSA) as more than 70% of the initial concentration were achieved via varying chitosan coat. It was observed that approximately 70% of the content is being released into Tris-HCl buffer, pH 7.4 within 24 h and no significant release of BSA was observed during treatment with 0.1M HCl pH 1.2 for 4 h. But the acid-treated beads had released almost all the entrapped protein into Tris-HCl pH 7.4 media within 24 h. Instead of BSA, the insulin preload was found to be very low in the chitosan/calcium alginate system; the release characteristics were similar to that of BSA. From scanning electron microscopic studies, it appears that the chitosan modifies the alginate microspheres and subsequently the protein loading. The results indicate the possibility of modifying the formulation in order to obtain the desired controlled release of bioactive peptides (insulin), for a convenient gastrointestinal tract delivery system. © 1996 John Wiley & Sons, Inc.     

The effect of bismaleimide resin on curing kinetics of epoxy–amine thermosets

An analysis of the cure kinetics of several formulations composed of diglycidyl ether of bisphenol-A (DGEBPA) and aromatic diamines, methylenedianiline (MDA) and diaminodiphenyl sulfone (DDS), in the absence and presence of 4,4′-bismaleimidodiphenylmethane (BM) was performed. The dynamic differential scanning calorimetry (DSC) thermograms were analyzed with the help of ASTM kinetic software to determine the kinetic parameters of the curing reactions, including the activation energy, preexponential factor, rate constant, and 60 min ½ life temperature. The effects of substitution of one curing agent for another, their concentration, and the absence and presence of BM resin and its concentration on curing behavior, ethalpy, and kinetic parameters are discussed. © 1996 John Wiley & Sons, Inc.     

Synthesis of nanostructured copper hexacyanidoferrate and its application in voltammeteric detection of salbutamol

Nanostructured copper hexacyanidoferrate has been synthesized and characterized using elemental analysis, atomic absorption spectroscopy, thermal and infrared spectral studies. The transmission electron microscopic studies of the synthesized material showed that it consisted of irregular oval and rod shaped particles with a size range 70–100 nm. Nanostructured copper hexacyanidoferrate modified glassy carbon electrode was characterized by cyclic voltammetery and nanostructured copper hexacyanidoferrate–carbon nanotube composite material modified glassy carbon electrode has been used for electrocatalytic oxidation of salbutamol. The electrode modified with composite material was found to reduce the peak potential of oxidation of salbutamol by nearly 90 mV.     

Studies on the effect of thiuram disulfide on NR vulcanization accelerated by thiazole-based accelerator systems

Thiuram disulfides form synergistic combinations with thiazole and thiazole-based accelerators, namely, N-cyclohexy-2-benzothiazole sulfenamide (CBS), 2-mercaptobenzothiazole(MBT), and 2-mercaptobenzothiazyl disulfide (MBTS). Unfortunately, widely used thiuram disulfides (TD) generate carcinogenic N-nitrosoamine. It is reported that the nitrosamines from N-methylpiperazine and dibenzylamine are free from this menace. So, some investigations were carried out with the binary combinations of each of bis(N-methylpiperazino)thiuram disulfide (MPTD), tetrabenzylthiuram disulnde (TBzTD), and tetramethyl-thiuram disulfide (TMTD) separately with CBS, MBT, and MBTS. It was observed that all the TD are activated by the CBS, MBT, or MBTS in the combinations studied. The intensity of activation is manifested in the enhancement of torque, modulus, tensile strength, cure rate, hardness, and decrease of elongation at break values and is very much dependent upon the ratio of the accelerators used. Considering the torque, modulus, tensile strength, and the elongation at break values, it apears that MPTD and TBzTD are capable of competing with the hitherto unbeaten TMTD as suitable accelerators for the vulcanization of rubber. Some investigations in respect to heat- and age-resistance behavior have also been carried out and the observed differences in the activities of various binary combinations have been explained through a mechanism. The results obtained with filled vulcanizates indicate that the binary systems comprising TD and MBTS provide fruitful results of which the TBzTD–MBTS combination seems to give the best cure and physical data for practical vulcanizates. © 1996 John Wiley & Sons, Inc.