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Issue-4_April - Asian Journal of Research in Chemistry (AJRC)

Issue-4_April - Asian Journal of Research in Chemistry (AJRC)

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1. Department <strong>of</strong> pharmaceutical analysis, Anurag pharmacy college, Ananthagiri(V), Kodad(M), Nalgonda (Dt),<br />

Andhra Pradesh, India.508206<br />

2. D.C.R.M. Pharmacy College, Inkollu, Prakasham Dist, Andhra Pradesh, India.<br />

ABSTRACT:<br />

A simple, reproducible and efficient high performance liquid chromatographic method was developed for<br />

simultaneous determ<strong>in</strong>ation <strong>of</strong> Irbesartan and Hydrochlorothiazide <strong>in</strong> tablets. A Hypersil pack BDS C18 column<br />

250X4.6 mm 5µ particle size <strong>in</strong> isocratic mode with mobile phase conta<strong>in</strong><strong>in</strong>g acetonitrile: Buffer (sodium acetate<br />

anhydrous) (55:45 v/v ) adjusted to pH 3.5 us<strong>in</strong>g ortho phosphoric acid. The flow rate was 1.0 ml/m<strong>in</strong> and effluent<br />

was monitored at 260 nm. The retention time and l<strong>in</strong>earity range for Irbesartan and Hydrochlorothiazide were (2.98,<br />

4.83 m<strong>in</strong>) and (5-200, 1-400 g/ml), respectively. The developed method was found to be accurate, precise and<br />

selective for simultaneous determ<strong>in</strong>ation <strong>of</strong> Irbesartan and Hydrochlorothiazide <strong>in</strong> tablet dosage form.<br />

KEYWORDS: Irbesartan, Hydrochlorothiazide, RP-HPLC, simultaneous determ<strong>in</strong>ation, Validation.<br />

A M<strong>in</strong>uscule Study <strong>of</strong> Global Warm<strong>in</strong>g on Acetobacter aceti-Elevated Temperature and Its Impact over the<br />

Industries<br />

L. Krishnasamy and K. Jayanthi……………………………………………………………………………………………..477<br />

Dept. <strong>of</strong> Biotechnology, H<strong>in</strong>dustan College <strong>of</strong> arts and science, Kellambakkam-603 103, Chennai, Tamil Nadu<br />

ABSTRACT:<br />

The aim <strong>of</strong> this study was to <strong>in</strong>vestigate the effect elevated temperature on A.aceti which converts ethanol to acetic<br />

acid <strong>in</strong> the presence <strong>of</strong> oxygen. A.aceti was <strong>in</strong>cubated at various temperatures like 37°C, 42°C, and 47°C for<br />

overnight. After exposure, the DNA content <strong>in</strong> each culture was determ<strong>in</strong>ed. The results showed that an <strong>in</strong>crease <strong>in</strong><br />

temperature like 42°C and 47°C produced a marked decrease <strong>in</strong> the DNA content when compared to the culture<br />

<strong>in</strong>cubated at 37°C. The expression <strong>of</strong> gene was confirmed us<strong>in</strong>g PCR. The PCR result showed that the gene citrate<br />

synthase <strong>of</strong> A.aceti was expressed <strong>in</strong> the culture <strong>in</strong>cubated at 37°C and a significant suppression <strong>of</strong> the gene citrate<br />

synthase was seen <strong>in</strong> the culture treated at 42°C and 47°C.Therefore the elevated temperature on A.aceti will<br />

significantly affect the various importance <strong>of</strong> the organism especially <strong>in</strong> v<strong>in</strong>egar production where A.aceti plays a<br />

vital role.<br />

KEYWORDS: A.aceti, elevated temperature, v<strong>in</strong>egar, citrate synthase gene<br />

Solubility Enhancement <strong>of</strong> Poorly Water Soluble Drug by Solid Dispersion Technique<br />

Ahmed Samir 1 , Nagia El-Megrab 1 , Hanaa A. Fattah 1 , Waleed Barakat 2 ……………………………………………483<br />

Departments <strong>of</strong> 1 Pharmaceutics, 2 Pharmacology, Faculty <strong>of</strong> Pharmacy, Zagazig University, Egypt.<br />

ABSTRACT:<br />

The objective <strong>of</strong> present was to improve the solubility <strong>of</strong> Clonazepam (CZP), poorly water soluble drug, by solid<br />

dispersion technique us<strong>in</strong>g Polyethylene glycol 6000 (PEG 6000) and Urea (UR) as carriers. The Solid dispersion<br />

was prepared by physical mix<strong>in</strong>g and solvent evaporation method. The <strong>in</strong>teraction <strong>of</strong> the Clonazepam with PEG<br />

6000 and UR was evaluated by the Fourier transform <strong>in</strong>frared (FTIR) spectroscopy; Differential scann<strong>in</strong>g<br />

Calorimetry (DSC) and X-ray diffraction patterns (XRD). The results from the FTIR and XRD analyses showed that<br />

Solid dispersion might exist <strong>in</strong> the amorphous form. A DSC result showed that the sharp melt<strong>in</strong>g po<strong>in</strong>t was<br />

completely disappeared suggest<strong>in</strong>g that the CZP molecularly dispersed <strong>in</strong> an amorphous form. Dissolution studies<br />

<strong>in</strong>dicate that dissolution rate was remarkably <strong>in</strong>creased <strong>in</strong> Solid dispersion as compared to the physical mixture and<br />

drug alone. Also the pharmacological studies <strong>of</strong> the selected formulations [(1:3 CZP : PEG 6000) and (1:2 CZP :<br />

Urea)] were performed. In conclusion PEG 6000 and UR can be a well utilized to <strong>in</strong>crease the solubility <strong>of</strong> poorly<br />

water soluble drugs.<br />

KEY WORDS: Clonazepam, solid dispersion, Polyethylene glycol 6000, Urea.

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