Is Damp Heat Degradation of c-Si Modules Essentially Universal?

Author(s):  
Reza Asadpour ◽  
Muhammad A. Alam
Keyword(s):  
Author(s):  
KRISHNAPHANISRI PONNEKANTI ◽  
K. SUNITHA

Objective: Azelnidipine (AZEL) and Telmisartan (TELM) combination is referred to the sufferers of hypertension. No analytical process has yet been mentioned for the TELM and AZEL combination analysis. We, therefore, have designed for its first time stability demonstrating methodology based on HPLC for analysing TELM and AZEL in the tablets and bulk. Methods: The assay of TELM and AZEL was get done on a 250 mm length C18 column (Supelco, 4.6 mm inner diameter, 5.0 μm particle size), and utilized 0.1M Na2SO4 (pH 3.6) and acetonitrile (55% volume:  45% volume) as the mobile solvents phase, at a stream rate 1.0 ml/min. HPLC recognition of TELM and AZEL was taken by a photodiode array sensor set at 258 nm. For validation of the stability demonstrating methodology proposed in terms of sensitivity, precision, specificity, linearity, device adequacy, robustness and accuracy, ICH directives were followed. Results: Calibration curves of TELM and AZEL were generated in the array of 20-60 µg/ml and 4-12 µg/ml with recovery percentage ranges of 99.62%-101.05% and 97.76%-100.17%, and detection limits of 0.020 µg/ml and 0.009 µg/ml, respectively. TELM and AZEL stability was inspected in the existence of acid, base, light, heat, and oxidation and it was realised to be more stable under oxidation degradation testing conditions employed when compared to acid, alkaline, photo, and heat degradation testing conditions applied. Conclusion: The observations demonstrated that the described HPLC stability demonstrating methodology was suitable for quantitating TELM and AZEL combination in tablets and bulk.


2006 ◽  
Vol 53 (2) ◽  
pp. 63-69
Author(s):  
Takashi ISHIBASHI ◽  
Mitsunobu KITAMURA ◽  
Eiichi MIYAGAWA ◽  
Katsuhisa TOKUMITSU ◽  
Akira TANAKA

2018 ◽  
Vol 8 (6) ◽  
pp. 1847-1851 ◽  
Author(s):  
Wenqin Shi ◽  
Mirjam Theelen ◽  
Veronique Gevaerts ◽  
Andrea Illiberi ◽  
Nicolas Barreau ◽  
...  

1993 ◽  
Vol 20 (3) ◽  
pp. 207-214 ◽  
Author(s):  
T. Sajjaanantakul ◽  
J.P. Van Buren ◽  
D.L. Downing
Keyword(s):  

1997 ◽  
Vol 43 (7) ◽  
pp. 1215-1222 ◽  
Author(s):  
Anton M H P van den Besselaar ◽  
Jacoline Neuteboom ◽  
Joyce Meeuwisse-Braun ◽  
Rogier M Bertina

Abstract To contribute to the development of a reference reagent for monitoring heparin therapy, a lyophilized partial thromboplastin time (PTT) reagent was prepared from synthetic dioleoylphosphatidylcholine, dioleoylphosphatidylserine, and dioleoylphosphatidylethanolamine, with colloidal silica as activator. The reagent, coded 91/558, was contained in sealed glass ampoules; it deteriorated in a heat degradation experiment, but its activity remained constant for at least 4 years when stored at −70 °C. Within- and between-run precision with this reagent complied with the requirements proposed by the International Committee for Standardization in Haematology (ICSH) Panel on PTT. The response of this reagent and of two other reagents to heparin added to pooled normal plasma was nonlinear. Citrated samples from 58 patients receiving intravenous heparin and from 24 apparently healthy volunteers were tested with reagent 91/558, with Automated APTT (Organon Teknika), with Manchester APTT reagent, with an anti-factor Xa assay, and with an anti-factor IIa assay. The correlation of APTT with anti-Xa and anti-IIa activity was poor. The best correlation was observed between reagent 91/558 and the Organon Teknika reagent. Correlations were improved when individual patients’ samples were replaced by pooled plasmas from heparinized patients, in whom the effect of oral anticoagulation was minimal. These results suggest that preparation of a lyophilized synthetic phospholipid reagent is feasible for use in monitoring heparin therapy.


2013 ◽  
Vol 19 (2) ◽  
pp. 213-219 ◽  
Author(s):  
Nitin Prajapati ◽  
Atul Shirkhedkar ◽  
Sanjay Surana

Lafutidine (LTD) is a histamine H2 receptor antagonist, with anti-ulcer and mucosal protective activity. A sensitive and selective stability-indicating reversed- phase high -performance thin-layer chromatography (RP-HPTLC)/Densitometry method is suggested for the determination of LTD in the presence of its acid, alkaline, oxidative and dry heat degradation products. Stress testing of LTD was done according to the International Conference on Harmonization (ICH) guidelines in order to validate the stability-indicating power of the analytical procedures. Stress testing demonstrated that LTD underwent acid, alkaline, oxidative and dry heat degradation; on the other hand, it showed stability towards neutral and photo degradation. Chromatography was performed on aluminum-backed silica gel 60 RP-18 F254 S plates with Methanol: Water: Triethylamine 8: 2: 0.5 (v/v) as mobile phase. Densitometric scanning was performed at 276 nm. The system gave compact bands for LTD (Rf 0.67 ? 0.02). Linear regression analysis data for the calibration plots discovered a good linear relationship with r2 > 0.99 in the working concentration range 500 to 3000 ng per band. The limits of detection and quantification were 23.51 ng and 71.26 ng, respectively. The developed method can routinely be used for analysis of LTD in bulk and pharmaceutical formulations.


Author(s):  
Mirjam Theelen ◽  
Mathieu Tomassini ◽  
Nicolas Barreau ◽  
Henk Steijvers ◽  
Annalisa Branca ◽  
...  

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