Rishabha Malviya

Emerging Trends in Noninvasive Insulin Delivery.

This paper deals with various aspects of oral insulin delivery system. Insulin is used for the treatment of diabetes mellitus, which is characterized by the elevated glucose level (above the normal range) in the blood stream, that is, hyperglycemia. Oral route of administration of any drug is the most convenient route. Development of oral insulin is still under research. Oral insulin will cause the avoidance of pain during the injection (in subcutaneous administration), anxiety due to needle, and infections which can be developed. Different types of enzyme inhibitors, like sodium cholate, camostat, mesilate, bacitracin, leupeptin, and so forth, have been used to prevent insulin from enzymatic degradation. Subcutaneous route has been used for administration of insulin, but pain and itching at the site of administration can occur. That is why various alternative routes of insulin administration like oral route are under investigation. In this paper authors summarized advancement in insulin delivery with their formulation aspects.

Modification of polysaccharides: Pharmaceutical and tissue engineering applications with commercial utility (patents)

Polymer modifications open new era for the development of polymers with requisite properties. Use of modified polymers is practically boundless. Different studies focus on biomedical applications of chemically modified polysaccharides. Development and utilization of modified polysaccharides get attention to be used as carrier for pharmaceutical drug delivery as well as tissue engineering scaffolds. Grafted polymer shows better cellular regeneration, signal transmission, diagnostic and imaging material than putative form. This review article aims to discuss various approaches to modify naturally derived polymer and their applications as pharmaceutical drug carrier and as a material for wound dressing and artificial cartilage due to better biophysical cues. Manuscript included various patents based on the applications of modified polymers and techniques used to modify polymers.

Biomedical Applications of Interpenetrating Polymer Network System

Interpenetrating polymer network (IPN) has been regarded as one of the novel technology in recent years show- ing the superior performances over the conventional techniques. This system is designed for the delivery of drugs at a predetermined rate and thus helps in controlled drug delivery. Due to its enhanced biological and physical characteristics like biodegradability, biocompatibility, solubility, specificity and stability, IPN has emerged out to be one of the excellent technologies in pharmaceutical industries. This article focuses mainly on the biomedical applications of IPN along with its future applicability in pharmaceutical research. It summarizes various aspects of IPN, biomedical applications and also in- cludes the different dosage forms based on IPN.

Kheri (Acacia chundra, family: Mimosaceae) gum: Characterizationusing analytical, mathematical and pharmaceutical approaches

BACKGROUNDnNatural polymers have been used in medical, pharmaceutical, cosmetic and food industry. They should be characterized before their possible applications in different industries.nnnOBJECTIVESnThe objective of this study was to characterize Kheri (Acacia chundra, family: Mimosaceae) gum using analytical, mathematical and pharmaceutical approaches.nnnMATERIAL AND METHODSnCrude Kheri gum (KG) was purified using distilled water as a solvent and ethanol as a precipitating agent. KG was characterized in terms of phytochemical screening, micromeritic properties, microbial load, ash value, rheological behavior, solid state 1H nuclear magnetic resonance (NMR), mass spectra and Fourier-transform infrared spectroscopy (FTIR) studies for their possible applications in food, cosmetics and pharmaceutical industry.nnnRESULTSnStudies show that KG contains carbohydrates, while protein, fat, volatile oils, alkaloids and glycosides are absent. 1% aqueous solution of polysaccharide showed 25.58 × 103 kJ/kg activation energy and 1.39 Reynolds number. Viscosity average molecular weight of purified gum was found 1.73 × 105 D. Thermodynamic parameters, i.e., change in enthalpy ΔHv and change in enthalpy ΔHv, were found to be 12.26 × 103 kJ/mol and 24.47 kJ/mol, respectively. Mathematical approach also determined the rod shaped conformation of KG in aqueous solution. IR spectroscopic study shows the presence of free (COO-) and esterified (COO-R) carboxylic acid, ether (C-O stretching), galacturonic acid and mannose in polysaccharide 1H NMR study predicts presence of tetrahydropyran hydrogen in molecule. Furthermore, KG was also characterized as a suspending agent using paracetamol as a model drug. Flow rate, pH, particle size and settling behavior of suspensions were evaluated. Initial particle size of dispersed phase particles does not change significantly after 45 days.nnnCONCLUSIONSnFrom the findings of the research it can be concluded that KG can be used as an excipient in cosmaceuticals and pharmaceuticals and its characteristic rheological behavior may attract rheologists.

Stability facilitation of nanoparticles prepared by ultrasound assisted solvent-antisolvent method: Effect of neem gum, acrylamide grafted neem gum and carboxymethylated neem gum over size, morphology and drug release

In present research, etoricoxib nanoparticles were prepared using newly developed ultrasonication assisted solvent-antisolvent method. Neem gum (NGP) and their semisynthetic derivatives NGP-g-Am (acrylamide graft copolymer of neem gum) and CMNGP (carboxymethylated neem gum) were used to provide stability to drug nanoprecipitates. In this research response surface methodology based on 32 factorial design was utilized to evaluate the effect of two independent variables (concentration of drug and polymer) over size and entrapment efficiency of nanoparticles (dependent variables). When compared with pure drug nanocrystals, polymer stabilized molecular composite nanoparticles were of smaller size and spherical shape. CMNGP stabilized composite nanoparticles shown smaller size hence better performance in terms of solubility and dissolution rate as compared to NGP and NGP-g-Am. As shown by zeta seizer analysis for the same concentration of drug and stabilizer, size of nanoparticles were found in the range of NGP-g-Amu202f>u202fNGPu202f>u202fCMNGP and reverse case was observed for dissolution rate. Contact angle determination easily predict better hydrophilicity of CMNGP than NGP followed by NGP-g-Am. DSC thermogram predict the amorphous nature of CMNGP than NGP and NGP-g-Am. SEM revealed spherical shaped and non-aggregation of nanoparticles. Prepared nanosuspension show no aggregation and Ostwald repining after 45u202fdays when ultrasonicated for 5u202fs. t90% of optimized formulations of NGP (N9), NGP-g-Am (A8) and CMNGP (C1) was found to be 249.46u202fmin, 296.63u202fmin and 223.39u202fmin and followed 1° order, Higuchi and 1° order kinetics of drug, respectively. Similarity factor analysis predict that release pattern of drug from three different polymer stabilized nanoparticles are significantly differ to each other. Particle size of nanoparticles was studied in presence of solvent and findings showed no change in size after 45u202fdays.