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Journal articles on the topic 'Solid dosage form'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Yamuna, Choudhary, Goyal Anju, and Vaishnav Rajat. "Process Validation of Solid Dosage Form." Pharmaceutical and Chemical Journal 7, no. 1 (2020): 46–54. https://doi.org/10.5281/zenodo.13952198.

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Process validation is an essential part for the safety of drug products and also to maintain the quality of the products. It is a fundamental component for assuring the quality system used by pharmaceutical industries. Process validation is the key element to ensure the identity, purity, safety, and efficacy of drug products. The process validation precisely focused on the aim and method of analysis. The Process validation reduces product recalls and troubleshooting assignments which results in more economical manufacturing process and quality products. In this article an overview is given on

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2

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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3

Andrews, Gavin P. "Advances in solid dosage form manufacturing technology." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 365, no. 1861 (2007): 2935–49. http://dx.doi.org/10.1098/rsta.2007.0014.

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Currently, the pharmaceutical and healthcare industries are moving through a period of unparalleled change. Major multinational pharmaceutical companies are restructuring, consolidating, merging and more importantly critically assessing their competitiveness to ensure constant growth in an ever-more demanding market where the cost of developing novel products is continuously increasing. The pharmaceutical manufacturing processes currently in existence for the production of solid oral dosage forms are associated with significant disadvantages and in many instances provide many processing proble

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4

Verma, Navneet Kumar, Uma Srivastava, Satya Prakash Singh, Shweta Yadav, and Pragya Mishra. "A Review on Solid Dosage form: Tablet." Scholars Academic Journal of Pharmacy 13, no. 06 (2024): 219–26. http://dx.doi.org/10.36347/sajp.2024.v13i06.003.

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Tablet is defined as solid pharmaceutical dosage form containing drug substance generally with suitable diluents and prepared by either compression or molding methods. Tablets remain popular as a dosage form because of the advantages afforded, both to the manufacturer (e.g. simplicity and economy of the preparation, stability, and convenience in packing, shipping and dispensing) and the patient. Because of their composition, method of manufacture or intended use, tablets present a variety of characteristics and consequently there are several categories of tablets. Tablet formulation and design

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5

Lee, Jaemin, Chanwoo Song, Inhwan Noh, Sangbyeong Song, and Yun-Seok Rhee. "Hot-Melt 3D Extrusion for the Fabrication of Customizable Modified-Release Solid Dosage Forms." Pharmaceutics 12, no. 8 (2020): 738. http://dx.doi.org/10.3390/pharmaceutics12080738.

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In this work, modified-release solid dosage forms were fabricated by adjusting geometrical properties of solid dosage forms through hot-melt 3D extrusion (3D HME). Using a 3D printer with air pressure driving HME system, solid dosage forms containing ibuprofen (IBF), polyvinyl pyrrolidone (PVP), and polyethylene glycol (PEG) were printed by simultaneous HME and 3D deposition. Printed solid dosage forms were evaluated for their physicochemical properties, dissolution rates, and floatable behavior. Results revealed that IBF content in the solid dosage form could be individualized by adjusting th

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6

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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7

Virmani, Reshu, Tarun Virmani, Charan Singh, Geeta Singh, and Sameer Rastogi. "Validation of Solid Dosage form (Tablets): A Review." Research in Pharmacy and Health Sciences 1, no. 1 (2015): 6–12. http://dx.doi.org/10.32463/rphs.2015.v01i01.02.

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8

Abdoh, A., M. M. Al‐Omari, A. A. Badwan, and A. M. Y. Jaber. "Amlodipine Besylate–Excipients Interaction in Solid Dosage Form." Pharmaceutical Development and Technology 9, no. 1 (2004): 15–24. http://dx.doi.org/10.1081/pdt-120027414.

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9

Moribe, Kunikazu, Noboru Sekiya, Takayuki Fujito, et al. "Stabilization mechanism of limaprost in solid dosage form." International Journal of Pharmaceutics 338, no. 1-2 (2007): 1–6. http://dx.doi.org/10.1016/j.ijpharm.2006.12.047.

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10

Mattes, Robert, Denise Root, Yinqi Zhou, Chaoju Xiao, James Johnson, and Atul Shukla. "NIR Prediction of Solid Dosage Form Dissolution Profiles." NIR news 20, no. 5 (2009): 10–11. http://dx.doi.org/10.1255/nirn.1136.

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11

Kornushk, V. F., I. V. Bogunova, A. A. Flid, O. M. Nikolaeva, and A. A. Grebenshchikov. "INFORMATION-ALGORITHMIC SUPPORT FOR DEVELOPMENT OF SOLID PHARMACEUTICAL FORM." Fine Chemical Technologies 13, no. 5 (2018): 73–81. http://dx.doi.org/10.32362/2410-6593-2018-13-5-73-81.

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The article deals with the application of the system approach for constructing informationalgorithmic support for the pharmaceutical development of solid dosage forms. Information modeling of the life cycle of pharmaceutical drug development has been carried out starting from the stage of studying the active pharmaceutical substance and ending with the utilization of the drug. These models are built in the IDEF0 nomination. A generalized block diagram is presented that reflects, in its most general form, the iterative process of developing a ready-made dosage form as applied to the further tra

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12

Khatoon, Shehnaz, Anmolpreet Singh, Pankaj Kumar, and Masrror Hashmi. "Review Article on Inprocess Problems and Evaluation Tests of Tablets Manufacturing." Journal for Research in Applied Sciences and Biotechnology 2, no. 3 (2023): 198–201. http://dx.doi.org/10.55544/jrasb.2.3.26.

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Tablets are the traditional over all medicinal dosage forms for solid dosages. A tablet is a solid pharmaceutical dosage form that is typically manufactured by compressing or moldings the medicinal component with appropriate diluents. They are easier to create than any other dosage form, but during manufacturing, a number of issues may occur that force the batch to be discarded. Post compression studies are also crucial before the dosage forms are put on the market. Modern standards and concepts that emphasize bioavailability, bioequivalence, and validation, among other things, have an impact

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13

Doye, Pakpi, Tanya Mena, and Nilimanka Das. "FORMULATION AND BIO-AVAILABILITY PARAMETERS OF PHARMACEUTICAL SUSPENSION." International Journal of Current Pharmaceutical Research 9, no. 3 (2017): 8. http://dx.doi.org/10.22159/ijcpr.2017.v9i3.18892.

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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. Suspensions contribute to pharmaceutical dosage form development by supplying drugs that are insoluble in all acceptable medium and often distasteful. Suspension translates such drugs into more bio-available form when compared to capsules, tablets, coated tablets, enteric coated tablets and sustained re

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14

Bozal-Palabiyik, Burcin, Bengi Uslu, Yalcin Ozkan, and Sibel A. Ozkan. "In-Vitro Drug Dissolution Studies in Medicinal Compounds." Current Medicinal Chemistry 25, no. 33 (2018): 4020–36. http://dx.doi.org/10.2174/0929867325666180322145335.

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After oral administration, drug absorption from solid dosage forms depends on the release of the drug active compounds from the dosage form, the dissolution or solubilization of the drug under physiological conditions, and the permeability across the gastrointestinal tract. Dissolution testing is an essential part of designing more effective solid dosage forms in pharmaceutical industry. Moreover, dissolution testing contributes to the selection of appropriate formulation excipients for improving the dosage form efficiency. This study aims to analyze in-vitro drug dissolution testing in solid

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15

Shrestha, J., A. Shrestha, B. Shrestha, et al. "Oral Solid Dosage form Modification in Community Pharmacies of Kavrepalanchok and Bhaktapur Districts of Nepal." Kathmandu University Medical Journal 20, no. 1 (2022): 29–37. http://dx.doi.org/10.3126/kumj.v20i1.49830.

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Background People may modify their oral solid dosage form of medicine to deal with problem faced during medicine administration. The modification of dosage form may adversely affect the quality, safety and efficacy of the medicine. Objective To investigate the causes and practices of oral solid dosage form modification among the consumers going to community pharmacies. Method A descriptive, cross-sectional study was conducted in five community pharmacies of Kavrepalanchok and Bhaktapur districts of Nepal. The consumers visiting these pharmacies for their oral solid dosage form of m

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16

Chirkova, M. V., D. K. Gulyaev, M. P. Chugunova, and V. D. Belonogova. "DEVELOPMENT OF A SOLID DOSAGE FORM WITH ADSORPTION ACTIVITY." Pharmacy & Pharmacology 8, no. 4 (2021): 233–41. http://dx.doi.org/10.19163/2307-9266-2020-8-4-233-241.

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Enterosorbents are produced in various dosage forms – powders, tablets, pastes, etc., some of them are also manufactured in the form of capsules. A water-soluble polysaccharide complex (WSPC) manifesting a pronounced adsorption activity, which determines the prospects for the development of dosage forms of sorbents, was obtained from the cones of European Spruce (Picea abies).The aim of the work is to develop a solid dosage form with an adsorption activity based on a water-soluble polysaccharide complex from the cones of European Spruce (Picea abies).Materials and methods. The samples of Europ

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17

Popa, Eliza Grațiela, Carmen Gafițanu, Andreea Crețeanu, and Lăcrămioara Ochiuz. "Minitablets – a modern trend in solid dosage form technology." Farmacist.ro 4, no. 201 (2021): 26. http://dx.doi.org/10.26416/farm.201.4.2021.5326.

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18

Vaja, Maulikkumar D., Bhoomi D. Patel, Krina A. Patel, and Ankit B. Chaudhary. "A Review on process validation of solid dosage form." Journal of Drug Delivery and Therapeutics 11, no. 4 (2021): 157–60. http://dx.doi.org/10.22270/jddt.v11i4.4880.

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Objective: The purpose of this work is to perform a study on concurrent validation of levonorgestrel tablet BP 0.03mg that will deliver process validation approach as a quality assurance means. The process validation program will be investigated so that the plan will be designed to the character of the procedure under study. This can be performed by checking and controlling the various critical in process parameters. Method: The samples from the three consecutive batches of levonorgestrel tablet 0.03mg are collected at the different stages of the manufacturing from dispensing, mixing, gr

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19

Brachtel, D., R. Joeres, and E. Richter. "Bioavailability of caffeine from solid and dissolved dosage form." Journal of Hepatology 9 (January 1989): S119. http://dx.doi.org/10.1016/0168-8278(89)90413-3.

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20

Perioli, Luana, Giuseppina D’Alba, and Cinzia Pagano. "New oral solid dosage form for furosemide oral administration." European Journal of Pharmaceutics and Biopharmaceutics 80, no. 3 (2012): 621–29. http://dx.doi.org/10.1016/j.ejpb.2011.12.011.

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21

Narang, Ajit S., Divyakant Desai, and Sherif Badawy. "Impact of Excipient Interactions on Solid Dosage Form Stability." Pharmaceutical Research 29, no. 10 (2012): 2660–83. http://dx.doi.org/10.1007/s11095-012-0782-9.

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22

Hlinak, Anthony J., Kamal Kuriyan, Kenneth R. Morris, Gintaras V. Reklaitis, and Prabir K. Basu. "Understanding critical material properties for solid dosage form design." Journal of Pharmaceutical Innovation 1, no. 1 (2006): 12–17. http://dx.doi.org/10.1007/bf02784876.

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23

Al-Gousous, Jozef, and Peter Langguth. "Oral Solid Dosage Form Disintegration Testing — The Forgotten Test." Journal of Pharmaceutical Sciences 104, no. 9 (2015): 2664–75. http://dx.doi.org/10.1002/jps.24303.

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24

Alotaibi, Badriyah Shadid, Muhammad Ahsan Khan, Kaleem Ullah, et al. "Formulation and characterization of glipizide solid dosage form with enhanced solubility." PLOS ONE 19, no. 2 (2024): e0297467. http://dx.doi.org/10.1371/journal.pone.0297467.

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Glipizide, a poor water-soluble drug belongs to BCS class II. The proposed work aimed to enhance the solubility of glipizide by preparing solid dispersions, using polyvinyl pyrrolidone (PVP) and polyethylene glycol (PEG). Solvent evaporation method was used for the preparation of glipizide solid dispersions. Solid dispersions were prepared in four different drug-to-polymer ratios i.e. 1:1, 1:2, 1:3 and 1:4. Mainly effect of three polymers (PVP K30, PVP K90 and PEG 6000) was evaluated on the solubility and dissolution of glipizide. The in-vitro dissolution of all prepared formulations was perfo

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25

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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26

Pathak, Deepa, Sunita Dahiya, and Kamla Pathak. "Solid dispersion of meloxicam: Factorially designed dosage form for geriatric population." Acta Pharmaceutica 58, no. 1 (2008): 99–110. http://dx.doi.org/10.2478/v10007-007-0048-y.

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Solid dispersion of meloxicam: Factorially designed dosage form for geriatric populationThe objective of the present work was to improve the dissolution properties of the poorly water-soluble drug meloxicam by preparing solid dispersions with hydroxyethyl cellulose (HEC), mannitol and polyethylene glycol (PEG) 4000 and to develop a dosage form for geriatric population. Differential scanning calorimetry, X-ray diffractometry, Fourier transform infrared spectroscopy and scanning electron microscopy were used to investigate the solid-state physical structure of the prepared solid dispersions. Hig

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27

Kaur, Simran, and Sunil Gupta. "Forensic evaluation of solid dosage form using a thermoanalytical method." Pharmaspire 14, no. 03 (2022): 109–15. http://dx.doi.org/10.56933/pharmaspire.2022.14214.

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In the present study, a generic dosage form of metformin hydrochloride was developed using deformulation of a marketed product. The excipients used in the marketed product were identified using thermospectral method such as differential scanning calorimetry (DSC). The marketed formulation contained metformin hydrochloride 850 mg. The ingredients present in the marketed dosage form after performing thermal analysis were identified as metformin hydrochloride, sodium carboxymethyl cellulose, microcrystalline cellulose, hydroxypropyl methyl cellulose, and magnesium stearate. DSC analyses of the in

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28

Shah, Nidhi, Anuja Rana, Shuchi Mitra, Usha Sharma, and Khem Chand Sharma. "A Comprehensive Exploration of Topical Dosage Form in Ayurveda: A Review." Scholars International Journal of Traditional and Complementary Medicine 7, no. 02 (2024): 19–25. http://dx.doi.org/10.36348/sijtcm.2024.v07i02.001.

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In order to effectively deliver drug molecules to their intended targets in the body, different dosage forms are utilized. Adapting dosage forms to the specific needs of the modern era and the condition of the disease can enhance the provision of healthcare to those in need, particularly through the use of herbal and traditional (Unani and Ayurvedic) products. Ayurveda employs various classifications of dosage forms, such as Aushadha kalpana and Ahara kalpana. Aushadha kalpana can be further categorized into Primary kalpana (Panchavidha kashaya Kalpana) and Secondary kalpana. These classificat

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S.G.Gavande, R.O.Sonwane A.D.Pichkewar S.S.Dorik. "REVIEW ON IMMEDIATE RELEASE DOSAGE FORM." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES o6, no. 04 (2019): 8509–18. https://doi.org/10.5281/zenodo.2652693.

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<em>Most popular immediate release dosage forms such as tablet, capsule and pellet.</em><em> Because of its convenience of self-administration, and simple to the manufacturing. The type of dosage from is some advantages such as improved stability of formulation. Improved bioavablity of Product. Rapid onset action and cost effective as compare to other dosage formulation. They disintegrant are selected as type of dosage and physical characteristics of drugs. </em><em>The basic approach used in development tablets, capsule and pellet as the use of some excipient like superdisintegrants, Bulking

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30

Rajiv Kumar, Kiranjeet Kaur Batth, Jaspreet Kaur, Jaspreet Kaur, Parminder Nain, and R. K. Dhawan. "A most convenient and patient compliance dosage form- Tablet." Journal of Biomedical and Pharmaceutical Research 9, no. 6 (2020): 13–19. http://dx.doi.org/10.32553/jbpr.v9i6.815.

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Tablet is defined as solid pharmaceutical dosage form containing drug substance generally with suitable diluents and prepared by either compression which is given as a single unit and are known as solid unit dosage form. Tablets remain popular as a dosage form because of the advantages afforded, both to the manufacturer (e.g. simplicity and economy of the preparation, stability, and convenience in packing, shipping and dispensing) and the patient. The excipients include diluents, Binders and adhesives, disintegrates, etc. Tablets vary in shape and differ greatly in size and weight depending on

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31

Saurabh, Swami* Shubham Tikait Swati Deshmukh. "Formulation And Evaluation of Ayurvedic Solid Dosage Form of Vati." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 1908–22. https://doi.org/10.5281/zenodo.15387758.

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The present research focuses on the formulation and evaluation of an Ayurvedic solid dosage form Vati, using Triphala (a classical combination of Haritaki, Bibhitaki, and Amla) and jaggery (Gud). Triphala is known for its rejuvenating, digestive, and antioxidant properties, while jaggery acts as a natural binder and sweetener with additional nutritional benefits. The study involves standardizing raw materials, preparing the Vati by traditional methods, and evaluating its physicochemical properties such as hardness, friability, weight variation, and disintegration time. The formulation exhibite

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32

Lou, Hao, Bo Lian, and Michael J. Hageman. "Applications of Machine Learning in Solid Oral Dosage Form Development." Journal of Pharmaceutical Sciences 110, no. 9 (2021): 3150–65. http://dx.doi.org/10.1016/j.xphs.2021.04.013.

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33

Nagy, Zs K., I. Wagner, A. Suhajda, et al. "Nanofibrous solid dosage form of living bacteria prepared by electrospinning." Express Polymer Letters 8, no. 5 (2014): 352–61. http://dx.doi.org/10.3144/expresspolymlett.2014.39.

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34

Desai, Parind Mahendrakumar, Griet Van Vaerenbergh, Jim Holman, Celine Valeria Liew, and Paul Wan Sia Heng. "Continuous manufacturing: the future in pharmaceutical solid dosage form manufacturing." Pharmaceutical Bioprocessing 3, no. 5 (2015): 357–60. http://dx.doi.org/10.4155/pbp.15.19.

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35

., Umed A. Nikam, Abhijit V. Jadhav ., V. R. Salunkhe ., and C. S. Magdum . "An Overview of Pharmaceutical Process Validation of Solid Dosage Form." Journal of Current Pharma Research 3, no. 2 (2013): 824–35. http://dx.doi.org/10.33786/jcpr.2013.v03i02.006.

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36

Choi, Sung-Up, and Seong-Wan Cho. "Formulation of Liquid Choline Alphoscerate as a Solid Dosage Form." Journal of the Korea Academia-Industrial cooperation Society 14, no. 12 (2013): 6324–29. http://dx.doi.org/10.5762/kais.2013.14.12.6324.

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37

Łaszcz, Marta, and Anna Witkowska. "Studies of phase transitions in the aripiprazole solid dosage form." Journal of Pharmaceutical and Biomedical Analysis 117 (January 2016): 298–303. http://dx.doi.org/10.1016/j.jpba.2015.09.004.

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38

Roggo, Yves, Morgane Jelsch, Philipp Heger, Simon Ensslin, and Markus Krumme. "Deep learning for continuous manufacturing of pharmaceutical solid dosage form." European Journal of Pharmaceutics and Biopharmaceutics 153 (August 2020): 95–105. http://dx.doi.org/10.1016/j.ejpb.2020.06.002.

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LEUENBERGER, H., B. ROHERA, and C. HAAS. "Percolation theory — a novel approach to solid dosage form design." International Journal of Pharmaceutics 38, no. 1-3 (1987): 109–15. http://dx.doi.org/10.1016/0378-5173(87)90105-0.

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Prem Kumar, G., A. R. Phani, Sai Aditya Pradeep, R. G. S. V. Prasad, and H. L. Raghavendra. "Preparation and Characterization of Nanofibrous Solid Dosage Form Containing Enrofloxacin." Analytical Chemistry Letters 4, no. 5-6 (2014): 364–71. http://dx.doi.org/10.1080/22297928.2014.1000964.

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Anushree Jambhalunkar, Anushree Jambhalunkar, Dr A. V. Chandewar Dr.A. V. Chandewar, Dr M. A. Channawar Dr. M. A. Channawar, and Kunal Deshmukh Kunal Deshmukh. "Formulation and Evaluation of Fast Disintegrating Oral Solid Dosage Form." International Journal of Pharmaceutical Research and Applications 10, no. 3 (2025): 654–68. https://doi.org/10.35629/4494-1003654668.

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The present research focuses on the formulation and evaluation of fast disintegrating tablets (FDTs) intended to enhance patient compliance, particularly for geriatric, pediatric, and dysphagic patients who experience difficulty in swallowing conventional tablets. The objective was to develop a solid oral dosage form that rapidly disintegrates in the oral cavity without the need for water, ensuring a quick onset of therapeutic action. Nifedipine, a calcium channel blocker used to treat hypertension and angina, was selected as the model drug due to its poor water solubility and the need for rap

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Kale, Megha K. Wagh Snehal A. Walunj Ankita A. Dhage Shubhangi S. Awari Monika S. Bhalekar S. M. Lamkhade. G. J. "Recent Advances In Oral Solid Dosage Form Formulation And Development." International Journal in Pharmaceutical Sciences 2, no. 10 (2024): 1075–91. https://doi.org/10.5281/zenodo.13955626.

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The most sensible, safest, and natural way to take medication is through the mouth. An overview of the most recent materials and technologies utilized to address issues with patient compliance, pharmaceutical release, absorption, and overall efficacy will be given in this article. Because of their superior patient compliance, portability, stability, and convenience of handling, tablets are the most often used solid oral dose form. Over time, tableting technology has made considerable advancements. This work seeks to shed light on advancements in tablet excipients, production procedures, analyt

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43

Sheena, U., KG Parthiban, and R. Selvakumar. "LYOPHILIZED INJECTION: A MODERN APPROACH OF INJECTABLE DOSAGE FORM." Journal of Drug Delivery and Therapeutics 8, no. 5 (2018): 10–18. http://dx.doi.org/10.22270/jddt.v8i5.1829.

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Now-a-days, lyophilized injection dosage form is extensively used to improve the bioavailability, stability, solubility and patient compliance. The lyophilized injection has considered as alternative to oral solid dosage forms for better patient compliance especially in bed ridden patients and for attaining maximum bioavailability, improved stability. The lyophilized injection reconstitute before injection to produce liquid injection. This review includes a detailed updated concept on lyophilized injection. Keywords: Lyophilized injection, parenteral, freeze drying

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Gadad, G. G., K. S. Gudaganatti, and V. S. Mannur. "PHYSICO CHEMICAL EVALUATION OF AVIPATTIKARA CHURNA AND ITS DEVELOPED FORM OF SYRUP." INDIAN DRUGS 52, no. 06 (2015): 38–42. http://dx.doi.org/10.53879/id.52.06.10110.

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Development and modification of Ayurvedic classical formulations into widely acceptable dosage forms is an important area to be focused in the present era. The designing of liquid dosage form has generally been emphasized on the basis of ease of administration to those individuals who have difficulty in swallowing solid dosage forms, specially in pediatric and geriatric group. Churna (powders) are the preferentially administered Ayurvedic formulations by oral route. Most of these powders are hygroscopic, bitter to taste and should be administered with suitable vehicle. Avipattikara Churna is o

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Murugesan, Senthilkumar, Byran Gowramma, Kaviarasan Lakshmanan, Veera Venkata Satyanarayana Reddy Karri, and Arun Radhakrishnan. "Oral Modified Drug Release Solid Dosage Form with Special Reference to Design; An Overview." Current Drug Research Reviews 12, no. 1 (2020): 16–25. http://dx.doi.org/10.2174/2589977511666191121094520.

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Oral drug delivery is the most widely utilized route of administration among all the routes that have been explored for systemic delivery of drugs via pharmaceutical products of different dosage form and this oral route provides maximum active surface area among all drug delivery system for administration of various drugs. The attractiveness of these dosage forms is due to awareness of toxicity and ineffectiveness of drugs when administered by oral conventional method in the form of tablets and capsules. Usually, conventional dosage form produces wide range of fluctuation in drug concentration

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Ankit, Lodhi* Kavita Lovanshi Rita Mourya. "A Review on Mouth Dissolving Film." International Journal of Pharmaceutical Sciences 3, no. 4 (2025): 3154–56. https://doi.org/10.5281/zenodo.15295920.

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Mouth dissolving film is the most advanced oral solid dosage form due to its flexibility and comfort in use. Mouth dissolving films are oral solid dosage form that disintegrate and dissolve within a minute when placed in mouth without taking water or chewing. This dosage form allows the medication to bypass the first pass metabolism so bioavailability of medication may be improved .Mouth dissolving film has potential to improve onset of action lower the dosing and eliminate the fear of chocking. This review gives an idea about formulation techniques, evaluation parameters, overview on packagin

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Mishra, Sushmita, Shalini Sharma, Sandeep Sahu, and Amrita Chourasia. "DEVELOPMENT OF GASTRORETENTIVE MUCOADHESIVE SOLID DOSAGES FORM CONTAINING AMOXICILLIN TRIHYDRATE AND RANITIDINE HCL FOR THE TREATMENT OF HELICOBACTER PYLORI INFECTIONS." Journal of Applied Pharmaceutical Sciences and Research 6, no. 1 (2023): 34–40. http://dx.doi.org/10.31069/japsr.v6i1.05.

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Mucoadhesion can be explored in the design of drug delivery system. Mucoadhesive drug delivery systems interact with the mucus layer covering the mucosal epithelial surface, and mucin molecules, thus increasing the residence time of the dosage form at the site of absorption. The drugs having local action or possessing maximum absorption in gastrointestinal tract (GIT) requires increased duration of stay in GIT. Gastroretentive Mucoadhesive solid dosages form containing Amoxicillin Trihydrate and Ranitidine HCL were formulated to prolong the residence time of the dosage form at the site of appl

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Kute, Vaibhav Ghansham, Rajeshwari Satish Patil, Vaishnavi Ghansham Kute, and Priti Dilip Kaluse. "Immediate-release dosage form; focus on disintegrants use as a promising excipient." Journal of Drug Delivery and Therapeutics 13, no. 9 (2023): 170–80. http://dx.doi.org/10.22270/jddt.v13i9.6217.

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Disintegrants are materials or mixtures of substances added in the drug formulations, which make easier dispersion or breakup of tablets and ingredients of capsules in small-scale particles for fast dissolution then it comes in contact with water in the GI tract. Immediate drug release dosage forms disintegrate rapidly after administration with an enhanced rate of dissolution. The superdisintegrants provide instantaneous disintegration of tablets after administration in the stomach. In this field, immediate-release liquid dosage forms and parenteral dosage forms have also been introduced for t

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Abramova, E. G., A. V. Komissarov, N. V. Sinitsyna, I. M. Zhulidov, and A. K. Nikiforov. "Production of solid dosage forms of immunoglobulin products." BIOpreparations. Prevention, Diagnosis, Treatment 21, no. 4 (2021): 244–55. http://dx.doi.org/10.30895/2221-996x-2021-21-4-244-255.

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At the moment, there are no scientific publications devoted to the technological aspects of production of immunoglobulin solid dosage forms. The aim of the study was to review Russian and foreign literature on production of immunoglobulin solid dosage forms, and present the results of the authors’ own research. The authors analysed data of the National Register of Medicines of the Russian Federation as of mid-2021 on the authorised medicines with a generic name ‘globulin in a solid dosage form’, and summarised their characteristics. They reviewed data on the qualitative and quantitative compos

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Prasad, U. Viplava, M. Syam Bab, and B. Kalyana Ramu. "Determination of Sapropterin Dihydrochloride in Solid Dosage form by Visible Spectrophotometry." Asian Journal of Pharmaceutical Analysis 7, no. 2 (2017): 75. http://dx.doi.org/10.5958/2231-5675.2017.00012.6.

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