Relevant bibliographies by topics / Semisolid Dosage Form

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Semisolid Dosage Form'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Semisolid Dosage Form"

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B, Yuvan, and Inniya C. "Nano Technology based Topical Semisolid Pharmaceutical dosage Forms." International Journal of Pharmacy and Biomedical Engineering 1, no. 1 (2014): 13–15. http://dx.doi.org/10.14445/23942576/ijpbe-v1i1p105.

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The pharmaceutical semisolid dosages are normally present in the form of paste, creams, gels, ointments. Generally these types of semisolid dosages are used only externally such as skin allergies, injuries, etc. The bases used in the semisolid pharmaceutical dosage are more sensitive to the skin. The topical semisolid medical dosages are spread smoothly on the body surface. It will react with the cells and injuries for long time because it adhered for long time. The main advantages of the semisolid dosage are it does not create side effects. This paper proposes the Nano technology based semiso
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Salve, Priyanka M., Shital V. Sonawane, Mayuri B. Patil, and Rajendra K. Surawase. "Dissolution and Dissolution Test Apparatus: A Review." Asian Journal of Research in Pharmaceutical Sciences 11, no. 3 (2021): 229–36. http://dx.doi.org/10.52711/2231-5659.2021.00037.

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Dissolution is an official test. These used by pharmacopeias for evaluating drug release of solid and semisolid dosages forms. The application of the dissolution testing ensures consistent product quality and to predict in vivo drug bioavailability. The dissolution test, in its simplest form, placing the formulation in a dissolution apparatus containing suitable dissolution medium, allowing it to dissolved specified period of time and then using appropriate rational method to determine the amount of drug. Dissolution test are probative and analysis like drug degradation profile, shelf-life stu
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Csóka, I., E. Bozsik, I. Erős, and T. L. Paál. "Regulatory aspects of semisolid dosage form design." European Journal of Pharmaceutical Sciences 32, no. 1 (2007): S9. http://dx.doi.org/10.1016/j.ejps.2007.05.019.

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Prathamesh, Regade* Nikita Patil Komal Bhusare Sardar Shelke Nilesh Chougule. "Evalution Tests Of Different Dosage Forms An Overview." International Journal of Pharmaceutical Sciences 2, no. 7 (2024): 673–87. https://doi.org/10.5281/zenodo.12721342.

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The pharmaceutical industry continually strives to develop and enhance drug delivery systems to meet the diverse needs of patients. This study undertakes a comprehensive evaluation of solid, liquid, and semisolid dosage forms commonly used in pharmaceutical formulations. The research encompasses a range of parameters, including physicochemical properties, stability, bioavailability, and patient acceptability, to provide a holistic view of these formulations. For Solid pharmaceutical formulations, like tablets and capsules, we explore factors impacting dissolution rates, disintegration, The imp
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Patil, P. B., S. K. Datir, and R. B. Saudagar. "A Review on Topical Gels as Drug Delivery System." Journal of Drug Delivery and Therapeutics 9, no. 3-s (2019): 989–94. http://dx.doi.org/10.22270/jddt.v9i3-s.2930.

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The clinical evidence indicates that topical gel is a safe and most effective treatment option for use in the management of skin related disease and used for local action to reduce the side effects associated with other conventional dosage form. Topical drug delivery systems include a large variety of pharmaceutical dosage form like semisolids, liquid preparation, sprays and solid powders. Most widely used semisolid preparation for topical drug delivery includes gels, creams and ointments. A gel is a cross-linked polymer network swollen in a liquid medium. Its properties depend strongly on the
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Kaushal, Dev, and Nikita Upadhyaya. "REVIEW ON OINTMENT." International Journal of Pharmaceutical Sciences and Medicine 7, no. 10 (2022): 30–38. http://dx.doi.org/10.47760/ijpsm.2022.v07i10.003.

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Ointments are semisolid dosage form which usually act as visco-elastic materials when shear stress is applied. They generally contain medicinal ingredients and are used to be applied externally to the body for therapeutic effect. Many therapeutic agents used for topical application to intact or broken skin or to mucous membranes are presented in the form of semisolid consistency variously designated as ointments, creams, pastes etc. It is used mainly as protective or emollient for the skin. The first step towards the goal is screening of plants used in popular medicine. Along with other dosage
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SAKATA, Osamu, Hiraku ONISHI, and Yoshiharu MACHIDA. "Development of Semisolid Dosage Form of Clonazepam for Oral Cavity Administration." YAKUGAKU ZASSHI 130, no. 1 (2010): 119–25. http://dx.doi.org/10.1248/yakushi.130.119.

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Bhinde, SonamSagar, SagarMahendrabhai Bhinde, VirendrakumarK Kori, SwapnilY Chaudhari, BiswajyotiJ Patagiri, and KalpnaS Patel. "Pharmaceutical validation of modified Chitraka Haritaki Avaleha: An ayurveda semisolid dosage form." Journal of Indian System of Medicine 9, no. 1 (2021): 33. http://dx.doi.org/10.4103/jism.jism_109_20.

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van Amerongen, I. A., H. A. G. De Ronde, and N. T. M. Klooster. "Physical-chemical characterization of semisolid topical dosage form using a new dissolution system." International Journal of Pharmaceutics 86, no. 1 (1992): 9–15. http://dx.doi.org/10.1016/0378-5173(92)90025-w.

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Joshi, Shruti B., Dr Bharti Umretia, and Prof Dr Bharat D. Kalsariya. "Standard Manufacturing Procedure of Dadrughni Vati (Lepa) and Its Modified Dosage Form Dadrughna Malahara: Tradition to Innovation." International Journal of Pharmaceutical Research and Applications 10, no. 1 (2025): 996–1005. https://doi.org/10.35629/4494-10019961005.

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Introduction: Herbo-mineral formulations, require systematic pharmaceutical procedures to ensure efficacy, safety, and consistency. The increasing global demand for high-quality Ayurvedic products necessitates the development of Standard Manufacturing Procedures (SMPs). This study aims to design and establish an SMP for two Ayurvedic formulations, Dadrughni Vati (Lepa) and Dadrughna Malahara, ensuring reproducibility and quality across multiple batches. Materials and Methods: The study involved the procurement, identification, and preparation. The preparation of Dadrughni Vati (Lepa) involved
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Dissertations / Theses on the topic "Semisolid Dosage Form"

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Jaganath, Nelesh. "The application of rheological techniques in the characterization of semisolids in the pharmaceutical industry." Thesis, Nelson Mandela Metropolitan University, 2004. http://hdl.handle.net/10948/380.

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Rheological characterization of pharmaceutical semisolids is of importance as it provides fundamental information required for the assessment of some of the final properties of a product such as viscosity, elasticity, quality and storage stability. The effect of formulation variables on product characteristics such as consistency and correlation of consumer evaluation of consistency can also be attained. (Ramachandran et al., 1999) This study focussed on using rheological techniques to fully characterize the properties of various semisolid formulations being developed or produced at a South Af
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Brown, Chandra Demona. "A method of sampling a finished semisolid dosage form." 2002. http://purl.galileo.usg.edu/uga%5Fetd/brown%5Fchandra%5Fd%5F200208%5Fms.

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Thesis (M.S.)--University of Georgia, 2002.<br>Directed by Anthony Capomacchia. For abstract see http://getd.galib.uga.edu/hold5yr/brown_chandra_d_200208_ms/brown_chandra_d_200208_ms.pdf. Includes bibliographical references (leaves 34-37).
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Books on the topic "Semisolid Dosage Form"

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Niazi, Sarfaraz K. Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Four, Semisolid Products. Taylor & Francis Group, 2020.

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Niazi, Sarfaraz K. Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Four, Semisolid Products. Taylor & Francis Group, 2020.

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Niazi, Sarfaraz K. Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Four, Semisolid Products. Taylor & Francis Group, 2020.

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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Four, Semisolid Products. Taylor & Francis Group, 2020.

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Book chapters on the topic "Semisolid Dosage Form"

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Mahato, Ram I., Ajit S. Narang, and Virender Kumar. "Semisolid Dosage Forms." In Pharmaceutical Dosage Forms and Drug Delivery, 4th ed. CRC Press, 2024. http://dx.doi.org/10.1201/9781003389378-26.

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Gurny, Robert, and Nikolaos A. Peppas. "Semisolid Dosage Forms as Buccal Bioadhesives." In Bioadhesive Drug Delivery Systems. CRC Press, 2024. https://doi.org/10.1201/9781003574484-8.

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Shah, Vinod P. "In Vitro Release from Semisolid Dosage Forms." In Percutaneous Absorption, 5th ed. CRC Press, 2021. http://dx.doi.org/10.1201/9780429202971-18.

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Parhi, Rabinarayan. "Recent Advances in the Development of Semisolid Dosage Forms." In Pharmaceutical Drug Product Development and Process Optimization. Apple Academic Press, 2020. http://dx.doi.org/10.1201/9780367821678-6.

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Ansari, Mohammed Tahir, Dipti Srivastava, Ola Asem Mahmoud Abdou Ali, Tung Wai Hau, Farheen Sami, and Md Saquib Hasnain. "Advances in semisolid dosage form." In Dosage Forms, Formulation Developments and Regulations. Elsevier, 2024. http://dx.doi.org/10.1016/b978-0-323-91817-6.00018-8.

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Singh, Somnath, Alekha K. Dash, and Satish Agrawal. "Semisolid Dosage Forms." In Pharmaceutics. Elsevier, 2024. http://dx.doi.org/10.1016/b978-0-323-99796-6.00019-9.

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"Semisolid Dosage Forms." In Pharmaceutical Dosage Forms and Drug Delivery. CRC Press, 2011. http://dx.doi.org/10.1201/b12122-27.

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"Semisolid Dosage Forms." In Pharmaceutical Dosage Forms and Drug Delivery. CRC Press, 2007. http://dx.doi.org/10.1201/b13576-24.

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Goel, Ms Neha. "Semisolid Dosage Forms-I." In Edited Book of Pharmaceutics – I [According to Latest Syllabus of B. Pharm-I Semester of Pharmacy Council of India]. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/nbennurepch20.

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Semisolid dosage forms are essential for topical drug delivery, offering targeted therapeutic effects and patient convenience. Among them, creams and gels are particularly popular due to their versatile applications and ease of use
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Tiwari, Mr Prabhakar Singh. "Semisolid Dosage Forms-I." In Edited Book of Pharmaceutics – I [According to Latest Syllabus of B. Pharm-I Semester of Pharmacy Council of India]. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/nbennurepch19.

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Semisolid dosage forms are pharmaceutical preparations that have a consistency between solid and liquid. They are intended for topical application to the skin or mucous membranes, where they provide localized or systemic effects. These forms include ointments, creams, gels, and pastes, each designed to deliver active ingredients effectively while providing protective and soothing properties.
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Conference papers on the topic "Semisolid Dosage Form"

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TSINTAVI, E. "A deep learning approach for automated inspection of 3D printed orodispersible films." In Innovative Manufacturing Engineering and Energy. Materials Research Forum LLC, 2024. https://doi.org/10.21741/9781644903377-3.

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Abstract. This work aims at demonstrating the applicability of additive manufacturing and machine vision technologies for the on-demand manufacture of customized medicinal products at the point of need, while conforming to fundamental quality guidelines such as cGood Manufacturing Practices (cGMPs), Quality by Design (QbD) as well as Quality Risk Management (QRM) and assuring product quality. The adopted approach combines a 3D printing process for orodispersible films and a deep neural network model in order to develop an automated quality control system for defect detection. The orodispersibl
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