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Relevant bibliographies by topics / Cross Povidone

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Journal articles
Dissertations / Theses
Book chapters

Academic literature on the topic 'Cross Povidone'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Cross Povidone"

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P, Adeppa, Gandikota Venkata Prakash, Purushotham G, and Sumesh Raja Shanmugapandi. "To Study and Compare the Effect of Pre-Operative Skin Preparation with Aqueous Povidone Iodine Only and in Combination with Alcoholic Chlorhexidine on Surgical Site Infection in Tertiary Care Hospital SVRRGGH, Tirupati." Journal of Evidence Based Medicine and Healthcare 8, no. 35 (2021): 3252–56. http://dx.doi.org/10.18410/jebmh/2021/591.

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BACKGROUND Even the normal skin of healthy humans usually harbours a rich bacterial flora, which are usually non-pathogenic. But these organisms always have a potential to cause infection of the surgical site. The aim of surgical site preparation with antiseptics is to remove microorganisms harbouring the skin surface to a lower level. Povidine iodine (iodophors) and chlorhexidine are the agents most often used for pre-operative surgical site antisepsis. In this study, we wanted to determine the efficacy of pre-operative skin preparation with aqueous povidone iodine alone and when used in comb

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Alqhtani, Alaa Saif, Abdulkarem Ali Ali Mohammed, Farouk Al-ghazaly, Ahmed Alareqi, and Anis Irmawati. "Prevention of oral cross-infection by using povidone-iodine compared with other antiseptic agents for orally transmitted diseases: A Review." Health Dynamics 1, no. 5 (2024): 170–77. http://dx.doi.org/10.33846/hd10506.

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The oral cavity is a high-risk infective site, and highly contagious diseases like viral infections are confirmed to be transmitted through it. Oral rinses are a very important and one of the most important objective methods and topical essential strategies to decrease the spread and transmission of contagious diseases. There is a gap in the literature regarding a comprehensive comparison between povidone-iodine and other formulations in terms of their effectiveness in preventing oral cross-infection and transmission of orally transmitted diseases. The authors performed a comprehensive literat

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M., Anusha, Varun Raj S., Krishna Srewe P.V., Divya Deepthi N., Evanjiline Ch., and Roopa Koteswari Ch. "Formulation and Development of Rosuvastatin Fast Dissloving Tablets using Natural Super Disintegrates." Research & Review: Drugs and Drugs Development 1, no. 2 (2019): 61–77. https://doi.org/10.5281/zenodo.3271091.

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<em>Rosuvastatin is in category of the drug class. It is used to treat high cholesterol and to block cardiovascular disease. The main aim of this study is to develop oral dispersible tablets of Rosuvastatin using different types of super disintegrates to enhance the disintegration and dissolution of Rosuvastatin to improve bioavailability of the drug. Many trials were made to prepare a satisfactory rosuvastatin oral dispersible tablet using direct compression and wet granulation method. Formulate tablets were examine with different parameters such as weight variation, hardness, friability, wet

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K., Ramanji Reddy* Dr.Chandaka Madhu Dr. Mohammed Omar Sachin Vanji Ahirrao P.Jhansi Lakshmi. "FORMULATION AND EVALUATION OF MOUTH DISSOLVING TABLETS OF FEXOFENADINE HYDROCHLORIDE." Indo American Journal of Pharmaceutical Sciences 04, no. 09 (2017): 3230–42. https://doi.org/10.5281/zenodo.967492.

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In the present work, mouth dissolving tablets of fexofenadine HCl were designed with a view to enhance patient compliance by direct compression method. The present work studied the effect of superdisintegrants on release rate of fexofenadine HCl in the form of fast disintegrating tablet. For the present study range of superdisintegrants in their different concentrations, were used. The superdisintegrants used were Magnesium stearate, Microcrystalline Cellulose, Cross Povidone, Sodium Starch Glycolate,and Cross Carmellose Sodium. The blends were prepared by direct compression technique. The tab

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Mary Violet Jeyapriya, S.D.Milling Tania, Sonali Rathore, Sheloni Missier, and Bevin Shaga. "Comparative Evaluation of Antibacterial Activity of Chlorhexidine, Povidone Iodine and Glutaraldehyde for Disinfection of Orthodontic Appliances - An In-Vitro Study." International Journal of Orthodontic Rehabilitation 14, no. 1 (2023): 44–54. http://dx.doi.org/10.56501/intjorthodrehabil.v14i1.675.

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Introduction: Orthodontist must take precautionary measures to protect patients from cross-infection by contaminated materials received from the manufacturers. To minimize the incidence of cross-infection prior to bonding an invitro study was done to assess the antibacterial activity of chlorhexidine, povidone iodine and glutaraldehyde. Aim: To compare the antibacterial activity of 2% chlorhexidine, 5% povidone iodine and 2% glutaraldehyde on orthodontic materials prior to bonding. Materials and methods: A total of 36 samples were included in this study. The main group consists of 3 disinfecta

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SINGH, RAVINDRA, SUNIL KUMAR, AVINASH K. KONDALKAR, and MURAREE LAL. "FORMULATION AND EVALUATON OF FLOATING TABLET OF CEFPODOXIME PROXETIL." Current Research in Pharmaceutical Sciences 10, no. 3 (2020): 47–57. http://dx.doi.org/10.24092/crps.2020.100303.

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Ideal once daily floating drug delivery system should release the drug for 24 hours and float up to 24 hrs. Once daily floating matrix tablet of Cefpodoxime proxetil should be release the drug for 24 hours to maintain the effective plasma level. All the formulations were prepared by using two different grades of HPMC (K100 and K4), cross povidone and MCC pH 101. HPMC is a matrix forming agent. All the formulations showed buoyancy lag time of less than 5 seconds regardless of concentration of HPMC K100 M, K4 and cross povidone. It may be due to the low density of tablet. The swelling index of H

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Mr.A.Anka, Rao* B. Ramya M.V.L.Bhavani P.Ramesh A.Praveen Kumar V.Vasu Naik Dr. A.Seetha Devi. "FORMULATION AND EVALUATION OF FAST DISSOLVING TABLETS OF METOPROLOL SUCCINATE." iajps,csk publications 04, no. 04 (2017): 866–71. https://doi.org/10.5281/zenodo.556113.

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In the present work efforts have been made to develop fast dissolving tablets of Metoprolol succinate using direct compression technique involving super disintegrants like cross povidone, sodium starch glycolate. The pre compression parameters like angle of repose, bulk density, true density, compressibility index are within the IP limit. The post compression parameters are acceptable and within the IP limit. In-vitro drug release at for all the formulations was found to be 95 to 99% and was satisfactory. The optimized formulation (F6,10%cross povidone) of drug release was found to be is 99% a

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Hassan, Mohamed M., Motaman Ahmed, Noon Mohamed, et al. "The Management Outcomes of Maxderm Hydrocolloid Dressing Compared to Povidone Iodine Dressing Post Elective Cesarean Section Operations in Omdurman Maternity Hospital." SAS Journal of Surgery 7, no. 10 (2021): 601–9. http://dx.doi.org/10.36347/sasjs.2021.v07i10.017.

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Background: Dressing of post-surgical procedures was mainly dependent on Povidone iodine and saline gauze dressing, with longer hospital stay and more frequent dressing times which lead to increase surgical sites infection rates. Patient and Methods: This study is an observational prospective comparative cross-sectional hospital-based study, was conducted at Omdurman Maternity Hospital from November 2020 till August 2021. Data were collected by standardized questionnaire and analyzed by using SPSS version 20. Results: A total of 196 patients who satisfied the inclusion criteria were included i

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A.B., Gangurde Mohammed Awais* V. A. Bairagi Abdurrahman Sanaurrehman Karishma Rajashri. "FORMULATION DEVELOPMENT AND IN VITRO EVALUATION OF FAST DISSOLVING TABLETS OF RAMIPRIL SOLID DISPERSION." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 08 (2018): 8409–16. https://doi.org/10.5281/zenodo.1411687.

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<em>Ramipril is a prodrug belonging to the angiotensin</em>-<em>converting enzyme </em>(<em>ACE</em>) <em>inhibitor which is metabolized to Ramiprilat in the liver and, to a lesser extent, kidneys</em>.<em>The poor solubility and wett</em> <em>ability of Ramipril leads to poor dissolution and variations in bioavailability</em>.<em>Solid dispersion of Ramipril was prepared using Hydroxy propyl β</em>- <em>cyclodextrin to improve water solubility</em>. <em>Prepared solid dispersion was shown improved solubility in water of 97</em>.<em>5 µg</em>/<em>ml</em>. <em>Fast dissolving tablets

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Yulianto, Heribertus Dedy Kusuma, Nunuk Purwanti, Trianna Wahyu Utami, et al. "Dealing with the high-risk potential of COVID-19 cross-infection in dental practice." Majalah Kedokteran Gigi Indonesia 6, no. 1 (2020): 1. http://dx.doi.org/10.22146/majkedgiind.56588.

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The World Health Organization reported that the SARS-CoV-2 virus has infected more than 5 million people around the world. Dental care providers and health care professionals need to be aware of the high-risk potential of crossinfection since the routes of virus transmission commonly happen through droplets and aerosols. This review aimed at collecting essential knowledge about the COVID-19 needed by dental practitioners. The review focused on the oral involvement in COVID-19, the role of oral transmission as the high-risk potential of cross-infection and recommended strategies to minimize the

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Dissertations / Theses on the topic "Cross Povidone"

1

Chaiyakunapruk, Nathorn. "Meta-analysis and cost-effectiveness analyses of chlorhexidine gluconate and povidone iodine use for the prevention of catheter-related bloodstream infection /." Thesis, Connect to this title online; UW restricted, 2001. http://hdl.handle.net/1773/7946.

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Book chapters on the topic "Cross Povidone"

1

Noothi, Sadhana, Narender Malothu, and P. Vishnu. "Formulation and Characterization of Bilastine Oral Disintegrated Tablets Using Natural and Synthetic Super Disintegrants." In Current Trends in Drug Discovery, Development and Delivery (CTD4-2022). Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/9781837671090-00361.

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Bilastine (BLS) is a second-generation H1- antihistamine that is approved recently for the symptomatic treatment of chronic urticaria. The present investigation was to develop oral disintegrating tablets of BLS to produce a fast onset of action. In this study, an attempt was made to compare the effect of different natural and synthetic super disintegrants on the release profile of the formulation. The formulations (BF1-BF15) of BLS oral disintegrating tablets were prepared by direct compression technique using synthetic and natural super disintegrants (Chitosan, Fenugreek mucilage, Sodium star

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