Biomedical subjects

Arvind Kumar Bansal

Publications and source records attributed to Arvind Kumar Bansal.

4 recordsLinked to original sources

PubMed2006

Effect of particle size and compression force on compaction behavior and derived mathematical parameters of compressibility.

PURPOSE: To analyze the influence of inherent densification and deformation properties of paracetamol on the mathematical parameters derived from Heckel, Walker, Kawakita, and Adams equations and to correlate these with single particle nominal fracture strength and bulk compression parameters using confined compression on a fully instrumented rotary tablet press. MATERIALS AND METHODS: Force-displacement data were captured during in-die compression for four different particle size fractions (150-250, 300-450, 500-650, and 700-1,000 microm) of paracetamol each at compression force of 5.2, 8.6, and 17.3 kN. Nominal single particle fracture strength was obtained by micro tensile testing. RESULTS: Apparent mean yield pressure (Py) from Heckel analysis was significantly affected by the applied pressure, and was influenced by elastic energy and Young's modulus. The single particle fracture strength correlated to parameters obtained from Heckel, Walker, Kawakita, and Adams equations. Results obtained from bulk compression and single particle measurements were consistent with, and polynomially related to Py, Kawakita (1/b), and Adams parameter (tau0'). CONCLUSIONS: Values of Py, 1/b, and tau0' obtained from Heckel, Kawakita, and Adams equations, respectively, can be interpreted as a measure of single particle nominal fracture strength during confined compression loading. Walker and Adams parameters were less affected, than Heckel and Kawakita parameters, by the applied pressure.

Acetaminophen↗

PubMed2006

Development and validation of isomer specific RP-HPLC method for quantification of cefpodoxime proxetil.

The present work explains the development and validation of a simple and reliable isomer specific liquid chromatographic method for the quantitative determination of cefpodoxime proxetil (CP) in rat in situ intestinal perfusate samples. Chromatography was carried out by reversed-phase technique on a C-18 column with a mobile phase composed of 20 mM ammonium acetate buffer (pH 5.0) and acetonitrile in the ratio of 62:38 pumped at a flow-rate of 1 ml/min. The detection was carried out at 235 nm and a column temperature of 30 degrees C. The method was evaluated for the various validation parameters, such as linearity, accuracy, precision, LOD, LOQ, specificity, selectivity, and sample stability. The results of intra- and inter-day validation (n = 3) showed the method to be efficient and the same was applied in an in situ permeability study conducted for CP in rats.

Animals↗

PubMed2006

Compression physics in the formulation development of tablets.

The advantages of high-precision dosing, manufacturing efficiency, and patient compliance make tablets the most popular dosage forms. Compaction, an essential manufacturing step in the manufacture of tablets, includes compression (i.e., volume reduction and particle rearrangement), and consolidation (i.e., interparticulate bond formation). The success of the compaction process depends not only on the physico-technical properties of drugs and excipients, especially their deformation behavior, but also on the choice of instrument settings with respect to rate and magnitude of force transfer. This review discusses various properties of drugs and excipients, such as moisture content, particle size and distribution, polymorphism, amorphism, crystal habit, hydration state, and lubricant and binder level of the blend that have an influence on compaction. Tableting speed and pre/main compression force profile, also have a bearing on the quality of the final tablet. Mechanistic aspects of tableting can be studied using, instrumented punches/dies, instrumented tableting machines, and compaction simulators. These have potential application in pharmaceutical research and development, such as studying basic compaction mechanism, process variables, scale-up parameters, trouble shooting problem batches, creating compaction data bank, and fingerprinting of new active pharmaceutical ingredients (APIs) or excipients. Also, the mathematical equations used to describe compaction events have been covered. These equations describe density-pressure relationships that predict the pressures required for achieving an optimum density. This understanding has found active application in solving the analytical problems related to tableting such as capping, lamination, picking, sticking, etc. Mathematical models, force-time, force-distance, and die-wall force parameters of tableting are used to describe work of compaction, elasticity' plasticity, and time dependent deformation behavior of pharmaceuticals. Various indices of tableting performance such as the bonding index, brittle fracture index, and strain index can be used to predict compaction related problems. Compaction related physico-technical properties of commonly used tableting excipients have been reviewed with emphasis on selecting suitable combination to minimize tableting problems. Specialized tools such as co-processing of API and excipients can be used to improve their functionality.

Chemistry, Pharmaceutical↗

PubMed2004

Amorphous drug delivery systems: molecular aspects, design, and performance.

The biopharmaceutical properties-especially the solubility and permeability-of a molecule contribute to its overall therapeutic efficacy. The newer tools of drug discovery have caused a shift in the properties of drug-like compounds, resulting in drugs with poor aqueous solubility and permeability, which offer delivery challenges, thus requiring considerable pharmaceutical manning. The modulation of solubility is a more viable option for enhancing bioavailability than permeability, because of the lack of "safe" approaches to enhance the latter. Solid-state manipulation in general, and amorphization in particular, are preferred ways of enhancing solubility and optimizing delivery of poorly soluble drugs. This review attempts to address the diverse issues pertaining to amorphous drug delivery systems. We discuss the various thermodynamic phenomenon such as glass transition, fragility, molecular mobility, devitrification kinetics, and molecular-level chemical interactions that contribute to the ease of formation, the solubility advantage, and the stability of amorphous drugs. The engineering of pharmaceutical alloys by solubilizing and stabilizing carriers, commonly termed solid dispersions, provide avenues for exploiting the benefits of amorphous systems. Carrier properties, mechanisms of drug release, and study of release kinetics help to improve the predictability of performance. The review also addresses the various barriers in the design of amorphous delivery systems, use of amorphous form in controlled release delivery systems, and their in vivo performance.

Adjuvants, Pharmaceutic↗