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Relevant bibliographies by topics / HPMC (15 cps)

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Academic literature on the topic 'HPMC (15 cps)'

Author: Grafiati

Published: 3 June 2025

Last updated: 19 July 2025

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Journal articles on the topic "HPMC (15 cps)"

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K., Rekha Rani* Y. Navya Reddy R. Mohana Priya. "FORMULATION AND EVALUATION OF SUSTAINED RELEASE DOSAGE FORM OF KETOPROFEN." indo American Journal of Pharmaceutical Sciences 04, no. 05 (2017): 1384–90. https://doi.org/10.5281/zenodo.804916.

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Sustained release Ketoprofen matrix tablets were prepared by direct compression method. The nature of the polymer influences the physical and release characteristics of the matrix tablet. The hydrophobic polymer, Ethyl cellulose has retarded the drug release from the tablet and the hydrophilic polymer, HPMC (15 cps) has release the drug. While making the combination of both hydrophilic and hydrophobic polymers i.e HPMC and Ethylcellulose with optimized ratio (F7) leads to sustained release of drug from matrix tablet for 12 hours was observed Key words: Ketoprofen, HPMC (15 cps), Ethyl cellulos

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2

Islam, Md Saiful, Md Ziaur Rahman Khan, Masuda Khatun, Jakir Ahmed Chowdhury, and Md Selim Reza. "Studies on Bio-adhesion of Matrix Tablets: II.Comparison on Bio-adhesion Strength and Release Profiles of Theophylline Anhydrous and Its Sodium Glycinate Salt." Dhaka University Journal of Pharmaceutical Sciences 10, no. 1 (2012): 1–7. http://dx.doi.org/10.3329/dujps.v10i1.10008.

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Controlled release matrix tablets of Theophylline anhydrous and Theophylline sodium glycinate were prepared with different types of bio-adhesive polymers e.g. HPMC 15 & 50 cps, Gelatin, PVP K-30, Na-CMC and Xanthan gum. Tablets, prepared by direct compression method were subjected to in-vitro drug dissolution for 8 hours in 0.1 N hydrochloric acid (pH 1.2) using a thermal shaker at 50 rpm at 37 ± 0.5ºC. The bio-adhesive property was investigated in terms of retention time following in-vitro wash-off method by Lehr et al. The anhydrous and corresponding salt form was used to investigate whe

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Akhila, Salla, and Dr U. Mohan Kumar. "Formulation and evaluation of a pH induced in situ occular gelling system of piroxicam." International Journal of Clinical Pharmacokinetics and Medical Sciences 5, no. 3 (2025): 21–29. https://doi.org/10.26452/ijcpms.v5i3.778.

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Poor ocular bioavailability is caused by the traditional liquid ophthalmic delivery systems' short pre-corneal residence time and relative corneal impermeability. Based on the concept of pH-induced in situ gelation, the current study aimed to develop and evaluate an ocular delivery system for the non-steroidal anti-inflammatory medication Piroxicam. Sodium alginate was used as the gelling agent in combination with HPMC (0.25-0.75% w/v), which acted as a viscosity-enhancing agent. Compatibility studies of the drug excipients were carried out using FTIR studies. Clearness, pH, gelation studies,

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Nadimpalli, Naga Anusha, and Sunitha Reddy, M. "Formulation and Evaluation of Olmesartan Medoxomil Transdermal Drug Delivery System." Saudi Journal of Medical and Pharmaceutical Sciences 8, no. 10 (2022): 518–26. http://dx.doi.org/10.36348/sjmps.2022.v08i10.005.

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Transdermal patches are cutting-edge drug delivery methods that are essential to the management of many diseases. Due to the avoidance of first pass metabolism the drug molecules are delivered into the systemic circulation at a controlled and predefined pace with the help of TDDS, which also helps to achieve efficient bioavailability. This study's goal was to create matrix-type Olmesartan medoxomil transdermal patches utilizing the solvent evaporation method and various polymer ratios, including HPMC 15 cps, HPMC 5 cps, and Eudragit S 100. Plasticizers like glycerin, propylene glycol, and PEG

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KODI SHRUTI and M. SUNITHA REDDY. "Preparation and characterization of quetiapine fumarate loaded transfersome as a novel drug delivery system." GSC Biological and Pharmaceutical Sciences 25, no. 2 (2023): 372–86. http://dx.doi.org/10.30574/gscbps.2023.25.2.0463.

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Modern medicine delivery techniques like transdermal patches are vital for treating numerous disorders. With the aid of TDDS, first pass metabolism is prevented, which aids in achieving effective bioavailability. Drug molecules are also released into the systemic circulation at a controlled and predetermined rate. The objective of this study was creating matrix-type Quetiapine fumarate loaded transdermal patches with water bath method using different polymers like HPMC 5 cps, HPMC 15 cps, and Ethyl cellulose in different ratios. Polyethylene glycol-400, Dimethyl sulfoxide (DMSO) as a plasticiz

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KODI, SHRUTI, and SUNITHA REDDY M. "Preparation and characterization of quetiapine fumarate loaded transfersome as a novel drug delivery system." GSC Biological and Pharmaceutical Sciences 25, no. 2 (2023): 372–86. https://doi.org/10.5281/zenodo.10610028.

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Modern medicine delivery techniques like transdermal patches are vital for treating numerous disorders. With the aid of TDDS, first pass metabolism is prevented, which aids in achieving effective bioavailability. Drug molecules are also released into the systemic circulation at a controlled and predetermined rate. The objective of this study was creating matrix-type Quetiapine fumarate loaded transdermal patches with water bath method using different polymers like HPMC 5 cps, HPMC 15 cps, and Ethyl cellulose in different ratios. Polyethylene glycol-400, Dimethyl sulfoxide (DMSO) as a plasticiz

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M., Shobana. "Formulation and Evaluation of Fast Dissolving Oral Films of Sitagliptin Phosphate by Solvent Casting Method." International Journal of Pharmacy and Biological Sciences (IJPBS) 13, no. 3 (2023): 106–15. https://doi.org/10.5281/zenodo.10430292.

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Abstract The aim of this research work was to formulate fast-dissolving oral films of sitagliptin phosphate for the treatment of diabetes mellitus. The fast dissolving films of sitagliptin phosphate were prepared by solvent casting method using film forming polymers HPMC E 15 and HPMC E 50 cps and PEG and propylene glycol are used as plasticizers. All the films prepared were evaluated for weight variation, thickness, folding endurance, percentage elongation, tensile strength, drug content, <em>In</em>-vitro disintegration time, in-vitro dissolution test, SEM analysis and stability studies. All

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Edityaningrum, Citra Ariani, Artika Tri Oktafiani, Lina Widiyastuti, and Dewa Ayu Arimurni. "Formulation and Evaluation of Silver Nanoparticles Gel." Indonesian Journal of Pharmaceutical Science and Technology 9, no. 2 (2022): 125. http://dx.doi.org/10.24198/ijpst.v9i2.35343.

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Silver nanoparticles are known to be able to penetrate the cell membranes of acne-causing bacteria andcause structural damages that result in bacterial cell death. Silver nanoparticles need to be formulated inthe form of a gel to make it easier to use. This study was conducted to synthesis the silver nanoparticlesand to formulate it in the form of gel. The synthesis of silver nanoparticles was carried out usingthe chemical reduction method with sodium citrate as a reducing agent and gelatin as a stabilizersolution. The characterization results of silver nanoparticles obtained a maximum wavelen

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Ananthu, Likhitha, and Anie Vijetha, K. "Formulation and Evaluation of Simvastatin Transdermal Drug Delivery System." Saudi Journal of Medical and Pharmaceutical Sciences 8, no. 10 (2022): 527–35. http://dx.doi.org/10.36348/sjmps.2022.v08i10.006.

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Transdermal patches are a cutting-edge drug delivery technology that is essential in the management of many disorders. As first-pass metabolism is avoided, TDDS can effectively increase bioavailability and aid in the delivery of drug molecules into the systemic circulation at a planned and controlled rate. This study's goal was to create matrix-type simvastatin transdermal patches utilising the solvent evaporation method and various polymer ratios, including HPMC 15 cps, HPMC E5, and Eudragit S 100. Plasticizers like glycerine, propylene glycol, and PEG 200 are utilised, along with solvents li

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Patil, Swapnil, Manojkumar M. Nitalikar, and Preeti Khulbe. "Design and Development of Nanoparticle Based Nanogel Formulation of Bixa Orellena Seed Extract." International Journal of Pharmaceutical Sciences and Nanotechnology(IJPSN) 18, no. 1 (2025): 7842–48. https://doi.org/10.37285/ijpsn.2025.18.1.11.

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Background: Bixa orellana is known to contain Bixin, which has been known for its antifungal, antibacterial, and anti-inflammatory properties. Topical drug delivery is a widely utilized approach for achieving defined and sustained release of drugs at the intended site of action. Objective: The goal of the study is to prepare a nanoparticle based nanogel formulation from Bixa orellana seed extract. The present research work involves the synthesis of silver nanoparticles using an environmentally harmless and economically efficient method, utilizing the extract obtained from the seeds of Bixa ore

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Conference papers on the topic "HPMC (15 cps)"

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Søndenå, Rune, Halvard Haug, Chang Chuan You, Junjie Zhu, and Marie Syre Wiig. "Evolution of defect densities with height in a HPMC-Si ingot." In 15th International Conference on Concentrator Photovoltaic Systems (CPV-15). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5123897.

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Reports on the topic "HPMC (15 cps)"

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พงษ์สามารถ, สุนันท์, วิมลมาศ ลิปิพันธ์, ธิติรัตน์ ปานม่วง, ไกรสีห์ อัมพรายน์, เครือวัลย์ เอกรักษาศิลปชัย та นิจศิริ เรืองรังษี. การพัฒนาสารโพลี่แซคคาไรด์จากเปลือกของผลทุเรียน เพื่อใช้ทางการเภสัชกรรม : รายงานการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2001. https://doi.org/10.58837/chula.res.2001.27.

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เจลโพลี่แซคคาไรด์ (PG) และเส้นใยโพลี่แซคคาไรด์ (PF) สกัดได้จากเปลือกแห้งของผลทุเรียน (Durio zibethinus L.) ได้สารสกัด PG และ PF ประมาณ 7.3% และ 15.1% ของเปลือกแห้งตามลำดับ การวิเคราะห์ธาตุ พบว่าประกอบด้วย carbon (C) hydrogen (H) และ oxygen (O) ในอัตราส่วนอะตอมเท่ากับ 2.9:5.7:3.2 และ 3.5:6.4:3.1 ใน PG และ PF ตามลำดับและไม่พบมี nitrogen (N) และ sulfur (S) ในโพลี่แซคคาไรด์ทั้งสองชนิด PG มีส่วนประกอบของเส้นใย 96.3+-0.7% ซึ่งไม่พบมีเส้นใยอยู่ใน PF ผลการวิเคราะห์เกลือแร่ใน PG และ PF พบมีองค์ประกอบของโซเดียม โปแตสเซียม แคลเซียม แมกนีเซียม และมีจำนวนน้อยมากของเหล็ก ทองแดงสังกะสีและแมงกานีส องค์ประกอบข

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