Relevant bibliographies by topics / Semi-solid dosage forms

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Semi-solid dosage forms'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Semi-solid dosage forms"

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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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Pandey, Shubham, Sujeet Pratap Singh, and Dr Tarkeshwar P. Shukla. "Review–Formulation Development of Semi-Solid Dosage Form." INTERANTIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENT 07, no. 09 (2023): 1–11. http://dx.doi.org/10.55041/ijsrem25878.

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Semi-solid dosage forms are generally found in medicines for all types of patients. Though, they have specific advantages, along with fast efficacy due to the devoid of dissolution time and quick absorption in the skin surface. Semi-solid formulations have been broadly used in pharmacy due to their high dosing adjustability, easy use off, and rapid onset of action. Keywords: Semi-solid dosage forms, Gels, Ointment, Cream
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Krishna Sailaja, A. "Study of Natural Excipients in Semi-Solid Dosage Forms." Journal of Clinical Case Reports and Studies 6, no. 2 (2025): 01–07. https://doi.org/10.31579/2690-8808/245.

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A significant proportion of pharmaceutical dosage forms are semi solid preparations. They serve as carriers for drugs that are topically delivered by way of the skin, cornea, rectal tissue, nasal mucosa, vagina, buccal tissue, urethral membrane, and external ear lining. This data collection's goal is to give readers a comprehensive understanding of the different tools, tactics, crucial process variables, and production and validation procedures processes specific to semisolid dosage forms.
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YAMAUCHI, Hitoshi. "Semi-solid Dosage Forms and Transdermal Drug Delivery System." Oleoscience 17, no. 11 (2017): 559–65. http://dx.doi.org/10.5650/oleoscience.17.559.

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Kanfer, Isadore, Seeprarani Rath, Potiwa Purazi, and Nyengeterai Amanda Mudyahoto. "In Vitro Release Testing of Semi-Solid Dosage Forms." Dissolution Technologies 24, no. 3 (2017): 52–60. http://dx.doi.org/10.14227/dt240317p52.

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Mariia, Velia, Ruban Olena, Khalavka Maryna, and Hohlova Larisa. "Research of the choice of the basis of a semi-solid medicine with a semi-solid extract of Feverfew (Tanacetum parthenium)." ScienceRise: Pharmaceutical Science, no. 1(29) (February 27, 2021): 51–59. https://doi.org/10.15587/2519-4852.2021.225764.

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<strong>The aim.</strong>&nbsp;To conduct the research on the choice of the basis for a mild drug with a semi-solid extract of feverfew for use in dermatology. <strong>Materials and methods.</strong>&nbsp;In the study of the solubility of a semi-solid extract of feverfew (SSFE) used the method of optical microscopy using a laboratory microscope &ldquo;Konus Academy&rdquo;. Determination of pH and homogeneity of the studied samples was performed according to the methods described in SPhU, Vol.1. The bioavailability of the model samples was investigated by diffusion in 3 % agar gel. Colloidal st
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Sahu, Yogesh, Arvind Singh Jadon, Prateek Jain, Bhupendra Singh Thakur, Basant Khare, and Anushree Jain. "An Overview on Recent Advances in Pharmaceutical Suspensions." International Journal of Medical Sciences and Pharma Research 7, no. 1 (2021): 1–3. http://dx.doi.org/10.22270/ijmspr.v7i1.54.

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The suspension is a biphasic liquid or semi-solid dosage form where the finely divided insoluble solid drug particles are homogeneously dispersed in a liquid or semi-solid medium. The solid drug particles act here as the dispersed phase and the liquid or the semi-solid as the dispersion medium. The particle diameter in a suspension is usually greater than 0.5 µm. However, it is difficult and also impractical to impose a sharp boundary between the suspensions and the dispersions having finer particles. Suspensions are an important class of pharmaceutical dosage forms. The advantages of suspensi
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Schwarz, E., and S. Pfeffer. "Use of subambient DSC for liquid and semi solid dosage forms." Journal of Thermal Analysis 48, no. 3 (1997): 557–67. http://dx.doi.org/10.1007/bf01979502.

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Haverkamp, Jan Boris, Uwe Lipke, Thomas Zapf, Rudolf Galensa, and Cornelia Lipperheide. "Contamination of semi-solid dosage forms by leachables from aluminium tubes." European Journal of Pharmaceutics and Biopharmaceutics 70, no. 3 (2008): 921–28. http://dx.doi.org/10.1016/j.ejpb.2008.06.012.

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Svіtlana, Bilous, and Kovalevskaya Inna. "Study of the stability of organoleptic and structural-mechanical indicators of semi-solid preparations with metal nanoparticles." ScienceRise: Pharmaceutical Science, no. 1(17) (February 28, 2019): 39–44. https://doi.org/10.15587/2519-4852.2019.158590.

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<strong>Aim.</strong>&nbsp;Research of the stability of organoleptic and rheological properties of semi-solid preparations with silver and gold nanoparticles. <strong>Methods.</strong>&nbsp;For the study of organoleptic parameters, a classic method for determining the stability with periodic control of dosage forms in two temperature regimens was used: 8-15 &deg;C (cool place) and 15-25 &deg;C (room temperature). To study the rheological characteristics of semi-solid preparations, a rotary viscometer with a system of coaxial cylinders was used. <strong>Results.</strong>&nbsp;We studied three m
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Dissertations / Theses on the topic "Semi-solid dosage forms"

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LI, TSUNG-TE, and 李宗德. "The physical stability study of preparation and processoptimization of semi solid dosage forms." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/97978383308738209012.

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碩士<br>嘉南藥理大學<br>藥學系<br>104<br>A skin delivery method has many advantages over injection or oral administration because it can avoid first-pass hepatic metabolism and provides patients with an easier and more convenient route for drug administration. Topical semi-solid dosage forms contain one or more active ingredients dissolved or uniformly dispersed in a suitable base and any suitable excipients. The main stability problems observed in base are bleeding and change in consistency due to aging. The study was to investigate the physical stability in preparation and process optimization of the b
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Book chapters on the topic "Semi-solid dosage forms"

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Gkaragkounis, Angelos, and Dimitrios G. Fatouros. "Semi-solid Extrusion 3D Printing for the Development of Dosage Forms for Special Patient Groups." In Nano- and Microfabrication Techniques in Drug Delivery. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-26908-0_6.

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Goel, Ms Neha. "Dosage Forms." 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/nbennurepch3.

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Dosage forms are the means by which drug molecules are delivered to sites of action within the body. They are essential for ensuring the safe, effective, and controlled delivery of medication to achieve the desired therapeutic effect. The introduction to dosage forms encompasses a wide range of formulations designed to meet various medical needs and patient preferences. Dosage forms are broadly classified based on their physical state and route of administration. The primary classifications include solid, liquid, and semi-solid forms. Solid dosage forms include tablets, capsules, powders, and
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Kumar, Keshav, Dr Rupali Sharma, Dr Satish Sardana, Mr Shekhar Sharma, and Dr M. Aamir Mirza. "DOSAGE FORM DESIGN." In Futuristic Trends in Pharmacy & Nursing Volume 3 Book 14. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bkpn14p1ch6.

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The design of dosage forms is a pivotal endeavour within the realm of pharmaceutical sciences, encompassing the intricate interplay between active pharmaceutical ingredients (APIs) and formulation components to achieve optimal therapeutic outcomes. This chapter delves into the multifaceted landscape of dosage form design, exploring the nuanced considerations that underpin the creation of effective, safe, and patient-centric drug delivery systems. Commencing with an introduction to dosage forms, the chapter elucidates the critical role they play in pharmaceuticals, encapsulating a diverse spect
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Khan, Zuber, Mrs Mumtaz, Mohd Anas Saifi, Rizwan Ahamad, and Asad Ali. "DOSAGE FORM DESIGN." In Futuristic Trends in Pharmacy & Nursing Volume 3 Book 13. Iterative International Publisher, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bgpn13p2ch1.

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Designing pharmaceutical dosage forms is a crucial field that tries to provide convenient, reliable, and safe drug delivery systems. By spanning the gap between active medication ingredients and their administration, this multidisciplinary sector ensures the best possible therapeutic results. Drug qualities, patient characteristics, administration method, release kinetics, and manufacturing considerations are taken into account while designing dosage forms. The design must take into consideration the various demands of patients across age groups, from difficulties with compliance in young chil
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Dhondibhau, Ghangale Gauri. "Topical Preparations." In A Text Book of Pharmaceutics for I Year Diploma in Pharmacy. THINKPLUS PHARMA PUBLICATIONS, 2024. http://dx.doi.org/10.69613/t4gjs095.

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Topical preparations are dosage forms designed for application to the skin or mucous membranes, offering localized drug delivery and systemic effects in some cases. This section covers various types of topical formulations, including creams, ointments, gels, and transdermal patches. The structure and barrier properties of the skin are discussed in relation to drug penetration and absorption. Formulation considerations for topical preparations, such as drug solubility, partition coefficient, and vehicle selection, are explored to optimize drug delivery. The role of penetration enhancers and the
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Gidwani, Bina, Priya Namdeo, Sakshi Tiwari, et al. "Lipoidal Carrier as Drug Delivery System." In Nanoparticles and Nanocarriers-Based Pharmaceutical Formulations. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815049787122010012.

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The delivery system plays a vital role in managing the pharmacokinetics and pharmacodynamics of a drug. The size of the carrier system contributes to its pharmacological action. Lipid-based carriers refer to the formulations containing a dissolved or suspended drug in lipidic excipients. Lipoidal systems as carriers are achieving heights due to their significant lipid nature and the size of particles in the delivery system. The micro/nano-sized lipid-based carriers possess versatility in improving the physic-chemical properties of drugs. Also, they are biocompatible and can be administered thr
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Bedse, Anjali, Deepa Singh, Shilpa Raut, et al. "Organogel: A Propitious Carman in Drug Delivery System." In Advances in Drug Delivery Methods [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.107951.

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A gel is a semi-solid formulation having an external solvent phase that is either apolar (organogels) or polar (hydrogels) that is immobilized inside the voids contained in a three-dimensional networked structure. Organogels are bi-continuous systems composed of apolar solvents and gelators. When used at a concentration of around 15%, the gelators form self-assembled fibrous structures that become entangled with one another, resulting in the formation of a three-dimensional networked structure. The resulting three-dimensional networked structure blocks the flow of the external apolar phase. St
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Saha, Gourab. "Capsules." In A Text Book of Pharmaceutics for I Year Diploma in Pharmacy. THINKPLUS PHARMA PUBLICATIONS, 2024. http://dx.doi.org/10.69613/ghtjh139.

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Capsules are versatile solid dosage forms that offer unique advantages in drug delivery and patient acceptance. This section covers both hard and soft gelatin capsules, exploring their composition, manufacturing processes, and applications. The properties of gelatin and alternative shell materials, including vegetable-based and hydroxypropyl methylcellulose (HPMC) capsules, are discussed in relation to their impact on drug stability and release. Capsule filling processes for powders, granules, pellets, and liquids are examined, including manual, semi-automatic, and fully automatic filling meth
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Kaur, Simranjeet, Rajni Dhiman, and Pooja Sharma. "AN EMERGING PARADIGM FOR TOPICAL DRUG DELIVERY: EMULGELS." In Futuristic Trends in Pharmacy & Nursing Volume 3 Book 12. Iterative International Publisher, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bgpn12p5ch3.

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Semisolid mixes are the dermatological substances that get used superficially the most frequently. Topical drug delivery has a number of benefits, including the ability to self-medicate, preventing first-pass metabolism, lowering degradation, and enhancing patient compliance. These delivery methods can be found in a variety of solid, semi-solid, and liquid formulations, including powdered materials, creams, ointments, lotions, emulsions, and powders. The physiochemical characteristics of the carrier and the medication, which affect the release rates of the medications, determine how effective
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