Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms (Drugs and the Pharmaceutical Sciences)

2009 ◽  
Vol 210 (3-4) ◽  
pp. 299-299 ◽  
Author(s):  
Bert Klumperman
2015 ◽  
Vol 352 (1) ◽  
pp. 59-65
Author(s):  
Adriana Fuliaş ◽  
Gabriela Vlase ◽  
Anamaria Todea ◽  
Titus Vlase ◽  
Ionuţ Ledeţi

Pharmaceutics ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 685
Author(s):  
Dóra Farkas ◽  
Lajos Madarász ◽  
Zsombor K. Nagy ◽  
István Antal ◽  
Nikolett Kállai-Szabó

In pharmaceutical sciences, visual inspection is one of the oldest methods used for description in pharmacopeias and is still an important part of the characterization and qualification of active ingredients, excipients, and dosage forms. With the development of technology, it is now also possible to take images of various pharmaceutical dosage forms with different imaging methods in a size range that is hardly visible or completely invisible to the human eye. By analyzing high-quality designs, physicochemical processes can be understood, and the results can be used even in the optimization of the composition of the dosage form and in the development of its production. The present study aims to show some of the countless ways image analysis can be used in the manufacturing and quality assessment of different dosage forms. This summary also includes measurements and an evaluation of, amongst others, a less studied dosage form, medicated foams.


Author(s):  
Sagar Suman Panda ◽  
Ravi Kumar B V V ◽  
D Patanaik

A simple, precise and accurate spectrophotometric method was developed for analysis of the osteoporesis drug alendronate sodium (ALS). The method is based on reaction of the drug with sodium-1,2-naphthoquinone-4-sulphonate (NQS) in presence of alkali to form a brown colored complex giving absorption maximum at 525 nm. The drug obeyed Beer’s law in the range of 5-70 µg/ml with a correlation coefficient of 0.999. The LOD and LOQ values are 1.7 µg/ml and 5.0 µg/ml, respectively. The average recoveries for recovery study were found to be in the range of 99.37%-100.46%. The R.S.D. values for intraday and inter-day precision were found to be 0.48 and 0.62, respectively. The optimized assay conditions were applied successfully for determination of ALS in pharmaceutical dosage forms. No interference was observed from the excipients present in the dosage form. The method is statistically validated as per the ICH requirements.  


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