Preparation and evaluation of poly [caprolactone fumarate] nanoparticles containing doxorubicin HCl

Biodegradable Poly[caprolactone fumarate] [PCLF] has been used as bioresorbable sutures. In this study, doxorubicin HCl [Dox] loaded PCLF nanoparticles were prepared and characterized. PCLFs were synthesized by polycondensation of PCL diols [Mws of 530, 1250 and 2000] with fumaryl chloride. The degradation of PCLF in NaOH, water and phosphate buffer saline [PBS], was determined in terms of Mw. Nanoparticles [NPs] were prepared by two methods. In microemulsion polymerization method, dichloromethane containing PCLF and photoinitiator were combined with the water containing surfactants and then the mixture was placed under light for crosslinking. In nanoprecipitation method, the organic solvent containing PCLF was poured into the stirring water. The effect of several variables including concentration of PCLF, polyvinyl alcohol [PVA], Dox and Trypan blue [Trb] and the Mw of PCLF and PVA on NP size and loading were evaluated. PCLF 530, 1250 and 2000 in PBS or water were not degraded over 28 days. Nanoprecipitaion method gave spherical [revealed by SEM images] stable NPs of about 225 with narrow size distribution and a zeta potential of-43 mV. The size of NP increased significantly by increase in Mw or concentration of PCLF. Although PVA was not necessary for formation of NPs, but it decreased the NP size. Dox loading and EE were 2.5-6.8% and 15-20%, respectively. Increasing the drug concentration, increased the drug loading [DL] and NP size. The entrapment efficiency [EE] for Trb ranged from 1% for PCLF530 to 6% for PCLF2000. An increase in PCLF concentration resulted in an increase in EE. Dox and Trb release showed a burst followed by 80% and 78% release during 3 and 4 days respectively. PCLF possessed suitable characteristics for preparation nanoparticulate drug delivery system including desired NP size, stability and degradation time. Although PCLF530 NPs were the smallest, but their DL were lower than PCLF1250 and 2000 NPs

Simultaneous spectrophotometric determination of paracetamol, phenylephrine and chlorpheniramine in pharmaceuticals using chemometric approaches

The linear multivariate calibration models such as principal components regression [PCR] and partial least squares regressions [PLS1 and PLS2] due to the mathematical simplicity and physical or chemical interpretability are sufficient and generally preferred method for analysis of multicomponent drugs. In this study, simultaneous determination of paracetamol, phenylephrine and chlorpheniramine in pharmaceuticals using chemometric methods and UV spectrophotometry is reported as a simple alternative technique. Principal components regression [PCR] and partial least squares regressions [PLS 1 and PLS2] were used for chemometric analyses of data obtained from the spectra of paracetamol, phenylephrine and chlorpheniramine between wavelengths of 200 to 400 nm at several concentrations within their linear ranges. The analytical performance of these chemometric methods were characterized by relative prediction errors and recoveries [%] and compared with each other. PCR, PLS1 and PLS2 were successfully applied to a tablet formulation, with no interference from excipients as indicated by the recovery. However, the PLS1 shows better results due to its flexibility and mathematical principals. The proposed methods are simple and rapid requiring no separation step, and can be easily used as an alternative in the quality control of drugs