David, S (2019) Formulation and Compatibility of Admixture Study for Sodium Nitroprusside Infusion. Masters thesis, RVS College of Pharmaceutical Sciences, Coimbatore.
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Abstract
Admixture study was performed by diluting exhibit batch samples of Sodium Nitroprusside Injection 50 mg/2mL-2mL and RS NITROPRESS samples with 5% w/v Dextrose injection diluents present in 250 mL and 1000 mL infusion bags, accordingly physical and chemical test parameters were evaluated. ➢ Initial time point Admixed samples in 5% w/v Dextrose injection 250 mL and 1000 mL infusion bag, are analysed at 0 hrs and 24 hrs after dilution for the test parameter Description, pH, Assay and Related Substances and the results are found within the acceptance criteria of specification. CONCLUSION: ➢ Based on the obtained results, it is confirmed that the admixed generic product is stable for 24 hours, after admixing with 5% Dextrose injection in 250 mL infusion bag and 1000 mL infusion bag. ➢ The results obtained for admixture study of RS - NITROPRESS injection batch Number: 690103F were compared with the results as obtained for admixture study of generic product batche for Sodium Nitroprusside Injection 50 mg/2mL-2mL, Batch and were found to be comparable.
Item Type: | Thesis (Masters) |
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Additional Information: | 261710752 |
Uncontrolled Keywords: | Formulation, Compatibility, Admixture Study, Sodium Nitroprusside Infusion |
Subjects: | PHARMACY > Pharmaceutics |
Depositing User: | Ramakrishnan J |
Date Deposited: | 19 May 2022 07:08 |
Last Modified: | 19 May 2022 07:08 |
URI: | http://repository-tnmgrmu.ac.in/id/eprint/20125 |
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