Search Results - "Mehta, Priti"

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    Impact of space environment on stability of medicines: Challenges and prospects by Mehta, Priti, Bhayani, Dhara

    “…•Complex spaceflight environment can lead to unexpected alteration in efficacy and stability of space medicines.•The knowledge regarding space radiation…”
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    Journal Article
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    Recent updates in the clinical trials of therapeutic monoclonal antibodies targeting cytokine storm for the management of COVID-19 by Patel, Shikha, Saxena, Bhagawati, Mehta, Priti

    Published in Heliyon (01-02-2021)
    “…Clinical studies have identified a cytokine storm in the third stage of disease progression in critical ill patients with coronavirus disease 2019 (COVID-19)…”
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    Journal Article
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    A Review on Forced Degradation Strategies to Establish the Stability of Therapeutic Peptide Formulations by Patel, Shikha, Vyas, Vivek K., Mehta, Priti J.

    “…Peptides are small polymers composed of 40 or fewer amino acids and are an increasingly important class of drugs. Therapeutic peptides are less immunogenic and…”
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    Influence of Peroxide Impurities in Povidone on the Stability of Selected β-Blockers with the Help of HPLC by Prachi, Saklecha, Komal, Chaudhary, Priti, Mehta J.

    Published in AAPS PharmSciTech (01-10-2017)
    “…A present study was conducted to investigate compatibility of β-blocker drugs( like atenolol, labetalol hydrochloride, bisoprolol fumarate, metoprolol…”
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    Current approaches for in vitro drug release study of long acting parenteral formulations by Dadhaniya, Tejas M, Sharma, Om Prakash, Gohel, Mukesh C, Mehta, Priti J

    Published in Current drug delivery (01-06-2015)
    “…Long acting parenteral formulations are preferred over conventional formulations for the treatment of chronic diseases. Prevalence of such diseases provoked…”
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    Journal Article
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    Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Quantification of 15 Organic Impurities of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide in Combined Dosage Form by Desai, Pritesh R., Mehta, Priti J., Chokshi, Avani B.

    Published in Chromatographia (03-05-2019)
    “…A novel, simple, robust and rapid reversed-phased high performance liquid chromatographic method has been developed for the separation and quantitative…”
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    Liquid Chromatographic Method Development for Quantification of Inorganic Nitrite and Nitrate Impurities from Nitroglycerin Drug Substance by Using Ion-Pair Reagents with Liquid–Liquid Extraction Technique by Desai, Pritesh R, Mehta, Priti J, Chokshi, Avani B

    Published in Journal of chromatographic science (01-01-2020)
    “…Abstract A large number of laboratory studies have reported Nitrite (NO2−) and Nitrate (NO3−) to be among the most common degradation products of the…”
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  9. 9

    Correction to: Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Quantification of 15 Organic Impurities of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide in Combined Dosage Form by Desai, Pritesh R., Mehta, Priti J., Chokshi, Avani B.

    Published in Chromatographia (01-09-2019)
    “…The authors would like to call the reader’s attention to the following change in the corresponding authorship to Priti J. Mehta and Pritesh R. Desai’s…”
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    Journal Article
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    Physical Instabilities of Therapeutic Monoclonal Antibodies: A Critical Review by Bana, Arpit Arun K, Mehta, Priti, Ramnani, Khushboo Ashok Kumar

    “…The proteinaceous nature of monoclonal antibodies (mAbs) makes them highly sensitive to various physical and chemical conditions, thus leading to instabilities…”
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    Comparative stability study and aggregate analysis of Bevacizumab marketed formulations using advanced analytical techniques by Bana, Arpit Arunkumar, Sajeev, Nithin, Halder, Sabyasachi, Abbas Masi, Haidar, Patel, Shikha, Mehta, Priti

    Published in Heliyon (01-09-2023)
    “…Bevacizumab (Bvz) is the most preferred recombinant humanized monoclonal antibody in biosimilar development due to its prominence as a standard treatment in…”
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    Accelerated stability testing of levosimendan: isolation and characterization of degradation impurities utilizing preparative HPLC, LC-MS, NMR, and IR by Prajapati, Pintu B., Bhayani, Dhara R., Mehta, Priti J.

    “…Levosimendan (LEV) is an inodilator, mainly used for the short-term treatment of acutely decompensated congestive heart failure. Accelerated stability studies…”
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    Identification and structural characterization of major degradation products of tapentadol by using liquid chromatography-tandem mass spectrometry by Omkar, Sherikar D., Komal, Chaudhary, Priti, Mehta J.

    “…Tapentadol, a centrally acting analgesic was subjected to hydrolysis (acidic, alkaline, and neutral), oxidation, photolysis, humidity, and thermal stress…”
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    Effect of Phyllostachys parvifolia leaf extract on ionizing radiation-induced genetic damage: A preliminary in vitro cytogenetic study by Patel, Mansi, Mehta, Priti, Bakshi, Sonal, Tewari, Shikha

    “…The ionizing radiation is a known carcinogen as well as cancer therapeutic agent however, the side effect on normal tissue is a limiting factor and inadequate…”
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    ISOLATION AND CHARACTERIZATION OF RELATED IMPURITY IN MILNACIPRAN HYDROCHLORIDE ACTIVE PHARMACEUTICAL INGREDIENT by Khatri, Deepak M., Mehta, Priti J.

    “…Milnacipran hydrochloride is an antidepressant drug, belonging to a class of selective serotonin re-uptake inhibitors. Unknown impurity in active…”
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    Nondestructive and rapid concurrent estimation of paracetamol and nimesulide in their combined dosage form using raman spectroscopic technique by Lakhwani, Gargi, Sherikar, O, Mehta, Priti

    Published in Indian journal of pharmaceutical sciences (01-03-2013)
    “…A rapid, nondestructive Raman spectroscopic method was developed for quantitative estimation of paracetamol and nimesulide in their combined dosage form. A…”
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    Similarity assessment of charge variants for bevacizumab biosimilar formulations using imaged capillary isoelectric focusing by Bana, Arpit, Mehta, Priti

    “…The imaged capillary isoelectric focusing method was developed and validated for charge variant analysis of the bevacizumab innovator product and its…”
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    Journal Article
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