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Journal articles on the topic 'Tablet Dosage Form'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Sharma, Satish Kumar, Anand Singh, Anil Bhandari, and Sudhir Singh. "Formulation and Evaluation of New Dosage Form of Calcium and Vitamin D." Asian Journal of Pharmaceutical Research and Development 8, no. 3 (2020): 235–37. http://dx.doi.org/10.22270/ajprd.v8i3.707.

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The aim of the research work was to develop a new dosage form (tablet in tablet) of calcium and vitamin D. In this research work vitamin D3 was used as vitamin D. This type of dosage form is very useful for elder people and children who have a week swallowing reflex. They have difficulty in swallowing tablets with water. In the present research work, pre-formulated and evaluated chewable tablets of calcium and vitamin D3 (from Formulation and Evaluation of Chewable Tablets of Calcium and Vitamin D) were taken and then moulded into a jelly like material under specified conditions of temperature

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2

Pratiwi, Puspa Dwi, Shesanthi Citrariana, and Baiq Maylinda Gemantari. "Bahan Tambahan dalam Sediaan Tablet: Review." Sinteza 3, no. 2 (2023): 41–48. http://dx.doi.org/10.29408/sinteza.v3i2.17472.

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Tablets are solid pharmaceutical dosage form without or with suitable excipients by press or compression manufacturing process. The excipient chosen can influence the product performance (physical properties and stability) and bioavailability. All excipients must be optimally selected to get the optimal formula of tablet dosage form. This article review aims to overview of excipient in tablet dosage form and their role in formulating tablet dosage form. this review article was written based on literature studies from electronic databases such as PubMed, ScienceDirect, and Google Scholar which

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3

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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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

Ganesh, U. Chavan* Payal V. Suradkar Trupti D. Hudekar. "A Comprehensive Review On: Tablet." International Journal in Pharmaceutical Sciences 2, no. 10 (2024): 794–805. https://doi.org/10.5281/zenodo.13936009.

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Tablets are the most commonly prescribed dosage form as offer a convenient form of drug administration provides dosage uniformity from tablet to tablet. Medicines are not just a science but an art, involving understanding the processes of life. Pharmaceutical oral solid dosage forms have been widely used for decades due to their convenience and suitability for systemic effects. Tablets, made from powders, granules, pellets, or film-coated units, are the most popular dosage form, accounting for 70% of ethical pharmaceutical preparations. They can be prepared using compression or moulding method

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Ganesh, U. Chavan1* Payal V. Suradkar2 Trupti D. Hudekar2. "A Comprehensive Review On: Tablet." International Journal in Pharmaceutical Sciences 2, no. 10 (2024): 794–805. https://doi.org/10.5281/zenodo.13963865.

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Tablets are the most commonly prescribed dosage form as offer a convenient form of drug administration provides dosage uniformity from tablet to tablet. Medicines are not just a science but an art, involving understanding the processes of life. Pharmaceutical oral solid dosage forms have been widely used for decades due to their convenience and suitability for systemic effects. Tablets, made from powders, granules, pellets, or film-coated units, are the most popular dosage form, accounting for 70% of ethical pharmaceutical preparations. They can be prepared using compression or moulding method

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7

Kailash Sahu, Vimlendu Kumar, Pooja Lodhi, and Bhaskar Kumar Gupta. "Different types of pharmaceutical tablets used for treatment of diseases." GSC Biological and Pharmaceutical Sciences 21, no. 2 (2022): 001–11. http://dx.doi.org/10.30574/gscbps.2022.21.2.0398.

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In modern age of revolution and development in drug delivery for better clinical effects conventional dosages form have still a strong grip and most popular in all kinds of medicinal preparation intended for oral use. To satisfy the need of growing market tablets dosages form have incorporated modernization in producing and some advanced tablet types. Modified release tablet formulations including, layered tablets such as In +--lay tablet, Bi-layered tablet, Medicated chewing gum, Tablet tarts, Pastilles, Lollipop, Tablet inserts, Clinicaps, Caplets, Child ecstasy tablet and Tablet in tablet a

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8

Kailash, Sahu, Kumar Vimlendu, Lodhi Pooja, and Kumar Gupta Bhaskar. "Different types of pharmaceutical tablets used for treatment of diseases." GSC Biological and Pharmaceutical Sciences 21, no. 2 (2022): 001–11. https://doi.org/10.5281/zenodo.7649131.

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In modern age of revolution and development in drug delivery for better clinical effects conventional dosages form have still a strong grip and most popular in all kinds of medicinal preparation intended for oral use. To satisfy the need of growing market tablets dosages form have incorporated modernization in producing and some advanced tablet types. Modified release tablet formulations including, layered tablets such as In +--lay tablet, Bi-layered tablet, Medicated chewing gum, Tablet tarts, Pastilles, Lollipop, Tablet inserts, Clinicaps, Caplets, Child ecstasy tablet and Tablet in tablet a

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9

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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10

Ritesh, Aher* Mayuri Bagul Niraj Gaikwad Yogesh Sharma Dr. Deepak Sonawane Dr. Dhanajay Patil. "Orodispersible Tablet: A Review." International Journal of Pharmaceutical Sciences 2, no. 5 (2024): 1309–16. https://doi.org/10.5281/zenodo.11277534.

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At present time, the oral route is the most common and easily administered the various types of dosage forms like tablets, capsules, syrups, suspensions, elixirs etc. but some patients (paediatrices, geriatrices, bed-ridden etc.) are faces the difficulties to swallow of these formulations. So our researches are delevoped the new type dosages form are known as the Orodispersible Tablet is most commonly and widely used system because increase the patient compilance of all types patients such as paediatrics, geriatrics etc., to increase the bioavailability, time of duration of effectiveness etc.

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11

Agam, Kumar Chaubey* Ashok Baghel Dinesh Sharma Yogendra Singh. "Formulation And Evaluation of Bi-Layered Tablet of Divalproex Sodium." International Journal of Pharmaceutical Sciences 3, no. 3 (2025): 501–13. https://doi.org/10.5281/zenodo.14993024.

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The pharmacokinetic advantage relies on the criterion that, drug release from the fast-releasing layer leads to a sudden rise in the blood concentration. However, the blood level is maintained at steady state as the release from sustained layer. Particularly bilayer tablets are commonly used to avoid chemical incompatibilities of formulation components by physical separation, and release profile. The tablet is the most widely used dosage form because of its convenience in terms of self-administration, compactness and ease in manufacturing.4 Tablets are solid dosage forms containing medicinal s

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12

Arora, Rimjhim, Kamal Singh Rathore, and Meenakshi Bharakatiya. "An Overview on Tablet Coating." Asian Journal of Pharmaceutical Research and Development 7, no. 4 (2019): 89–92. http://dx.doi.org/10.22270/ajprd.v7i4.547.

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Pharmaceutical solid dosage forms include tablets, pellets, pills, beads etc. Tablet is most commonly used pharmaceutical dosage form which has ease of administration. Tablets are coated for many reason such as masking odour, taste, colour of the drug, providing physical and chemical protection to drug, protecting drug from the gastric environment.Coating is a process by which a layer of coating material is applied to the surface of a dosage form. Coating may also contain active ingredient. There are various strategies for tablet coating which include sugar coating, film coating, and enteric c

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13

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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14

V., B. Khot* D.A. Bhagwat J. I. D'Souza S. S. Shelake S. V. Patil. "OPTIMIZATION OF GRANULATION TECHNIQUES FOR DEVELOPMENT OF TABLET DOSAGE FORM." Indo American Journal of Pharmaceutical Sciences 04, no. 12 (2017): 4626–39. https://doi.org/10.5281/zenodo.1123244.

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The purpose of this study was to optimize the best granulation techniques for development of tablet dosage form. The present study explains comparative study of different wet granulation techniques including Planetary mixer granulation, Rapid mixer granulation, Fluid bed granulation with Direct compression method. Similar formulations were used to evaluate Planetary mixer granulation, Rapid mixer granulation and Fluid bed granulation method. The granules prepared by different techniques were evaluated for particle size distribution, porosity, spherisity, bulk density, flow property and compres

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15

Satyajit, Panda, Mishra Bibaswan, and Behera Swayamprava. "Bi-Layer Tablets: An Emerging State of Art Technology in Dosage Form Design." Journal of Advances in Nanotechnology and its Applications 3, no. 2 (2021): 1–14. https://doi.org/10.5281/zenodo.5515151.

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<em>Despite significant advancements in dosage form design, oral route still remains the most favoured route of drug administration. Even now-a-days tablets have got more attention compared to other dosage forms because of simple, inexpensive, greater stability and most suitable nature of tablets. More recently major considerations in tablet sector have been focused on development of controlled and immediate release drug delivery systems. Many pharmaceutical manufacturers are giving more emphasis to bi-layer tablet sector now a day, because of several advantages like extension of patent, impro

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16

Kumar, Vishal, Attish Bhardwaj, Navdeep Singh, Kamya Goyal, and Shammy Jindal. "A Review on Tablet Dosage Form: Recent Advancements with Special Emphasis on Rapid Disintegrating Tablet." Asian Journal of Research in Pharmaceutical Sciences 11, no. 3 (2021): 237–46. http://dx.doi.org/10.52711/2231-5659.2021.00038.

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Tablets are the most commonly prescribed dosage form as offer a convenient form of drug administration provides dosage uniformity from tablet to tablet, stable over extended and diverse storage conditions, can be produced on high-speed compression, labelling, and packaging equipment. Advancements in technology and modification in standard compressed tablet are to achieve better acceptability as well as bioavailability. Various types of newer and more efficient tablets are developed to create a delivery system that is relatively simple to administration. In one sense osmotic pump systems are an

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17

Priyanka, Priyanka, Kapil Kumar, and Deepak Teotia. "A comprehensive review on pharmaceutical mini tablets." Journal of Drug Delivery and Therapeutics 8, no. 6 (2018): 382–90. http://dx.doi.org/10.22270/jddt.v8i6.2060.

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Mini-tablets represent a new trend in solid dosage form design, with the main goal of overcoming some therapeutic obstacles. Mini tablets are multiple unit dosage forms and are advantageous than pellets or any other oral dosage forms as they are easy to manufacture and stability problems are less. Offering some therapeutic benefits such as dose flexibility and combined release patterns. They do not require any solvent for their production and also local irritation can be avoided by the use of mini tablet Mini tablet offer several advantages like they can be manufactured relatively easily, They

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18

Ashok, Kumar Sharma, Pushpendra Singh Naruka Dr., Shankar Soni Mr., Mohit Khandelwal Mr., Shaneza Aman Ms., and Mehul Mr. "SUBLINGUAL TABLET- ADVANCEMENT IN TABLET DOSAGES FORM." International Journal of Current Pharmaceutical Review and Research 11, no. 2 (2019): 01–05. https://doi.org/10.5281/zenodo.12672960.

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Sublingual drug delivery is often an alternate and better choice of route in comparison to oraldrug delivery as sublingually administered dosage forms bypass hepatic metabolism. A rapidonset of pharmacological effect is usually desired for a few drugs, especially those utilizedin the treatment of acute disorders and need onset of action. Sublingual tablets disintegraterapidly and therefore the bit of saliva present is typically sufficient for achievingdisintegration of the dosage form including better dissolution and increased bioavailabilitywith effective therapeutic range. Sublingual tablets

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19

Asija, Dr Rajesh, Karishma Sharma, and Seema Yadav Trimukhe. "A Review on Development of Fast Dissolving Tablet and Approaches in Pharmaceutical Dosage of Atorvastatin." International Journal of Research and Review 9, no. 5 (2022): 15–22. http://dx.doi.org/10.52403/ijrr.20220504.

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Dosage form tablets and capsules in the current era still have gained considerable importance and acceptance by the formulation scientists, physicians, and the patients due to their numerous advantages which include easy self-administration and cost-effectiveness experienced by the patients. However, the drug delivery through the tablet dosage is no doubt, associated with potential drawbacks which include difficulty for the older and pediatric patients to swallow (dysphagia), low fraction of drug available for absorption in the bloodstream due to first-pass hepatic effect, and a slower therape

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20

Kumar Bhasin, Rakesh, Nirika Bhasin, and Pradip Kumar Ghosh. "Advances in Formulation of Orally Disintegrating Dosage Forms: A Review Article." Indo Global Journal of Pharmaceutical Sciences 01, no. 04 (2011): 328–53. http://dx.doi.org/10.35652/igjps.2011.33.

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Oral disintegrating tablets are solid dosage form containing medicinal substances which disintegrates rapidly, usually within a matter of seconds, when placed upon the tongue The products are designed to disintegrate or dissolve rapidly on contact with saliva, thus eliminating the need for chewing the tablet, swallowing an intact tablet, or taking the tablet with water. ODT is general form of nomenclature for tablets that disintegrate rapidly or instantly in the oral cavity. Other alias are Quick Dissolve, Rapid Dissolve, Rapid Disintegrating, Fast Disintegrating, Fast Melt, Flash Melt and Mou

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21

Hummler, Henriette, Susanne Page, Cordula Stillhart, et al. "Influence of Solid Oral Dosage Form Characteristics on Swallowability, Visual Perception, and Handling in Older Adults." Pharmaceutics 15, no. 4 (2023): 1315. http://dx.doi.org/10.3390/pharmaceutics15041315.

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Swallowability, visual perception, and any handling to be conducted prior to use are all influence factors on the acceptability of an oral dosage form by the patient. Knowing the dosage form preferences of older adults, as the major group of medication end users, is needed for patient-centric drug development. This study aimed at evaluating the ability of older adults to handle tablets as well as to assess the anticipated swallowability of tablets, capsules, and mini tablets based on visual perception. The randomized intervention study included 52 older adults (65 to 94 years) and 52 younger a

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Kumari, Satish, Anchal Puri, Dhruv Dev, DN Prasad, and ,. Monika. "A review on polymers in natural or modified form used in sustained release tablet." Journal of Drug Delivery and Therapeutics 9, no. 3-s (2019): 870–73. http://dx.doi.org/10.22270/jddt.v9i3-s.2843.

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Tablet is a solid dosage form which is used to deliver the drug to the body to make pharmacological action. The oral dosage form should disperse into small particles to deliver active ingredients in the body, the disperse time of the dosage form depends on the ingredients which are used in the tablet. To make the tablet disintegrate slow usually sustained release agents are used. The sustained release tablets helps in maintaining the drug concentration in the body for the higher time. In this review article various polymers of natural origin and their modified forms are studied, which can be u

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Kaur, Kiranpreet* and Garg Rajeev. "FAST DISSOLVING TABLET – AN INNOVATIVE APPROACH." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 10 (2018): 10603–11. https://doi.org/10.5281/zenodo.1469989.

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<em>Fast dissolving tablets are the most supportive and widely accepted dosage forms, commonly for pediatric patients. </em><em>Some solid dosage forms like capsules and tablets have issue like worry of swallowing called dysphagia, resulting in matter of patient non-compliance and making the therapy inefficient. FDT disintegrate or dissolve quickly in the saliva in lack of water in within a few seconds (less than 60 seconds) and are real fast dissolving tablets. FDTs are designed to disintegrate speedily, absorb faster so,in vitro drug release time improve and this property of drugs enhanced b

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Hongthong, Charkkrit, Rungpetch Sakulbumrungsil, Nusaraporn Kessomboon, et al. "Dosage form selection using price function of prediction market." F1000Research 14 (February 12, 2025): 197. https://doi.org/10.12688/f1000research.161732.1.

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Backgrounds A prediction market (PM) is a process for predicting future events by gathering knowledge from participants. Researchers applied PM concept to predict the new dosage form, the industry may be able to produce incrementally modified drugs (IMDs) in the future. Methods The PM process started with building a PM based on the market scoring rule, which is a mechanism that automatically adjusts prices through the calculation of the price function by the market maker. Analysis of data according to the PM process. Since March 19, 2022, participants in Thailand’s pharmaceutical industry have

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25

Pawar, Tejal, Raj Chitte, Sanjivani Bachhav, Deepali Deore, and Prajakta Bachhav. "A Review on Sublingual Dosage Form." International Journal for Research in Applied Science and Engineering Technology 13, no. 1 (2025): 1095–100. https://doi.org/10.22214/ijraset.2025.66524.

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Abstract: A sublingual tablet is a medication formulation that dissolves beneath the tongue, facilitating quick absorption of the active ingredients through the mucous membranes and into the bloodstream. Bypassing the liver metabolism and digestive tract, this technique can improve the effectiveness and speed of medication delivery. Sublingual medications are frequently used for drugs that need to start working quickly. Benefits of the sublingual route include a more consistent therapeutic impact and the avoidance of stomach upset. The salient features of the sublingual tablet include its abil

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Deshmukh, Komal* Narsale Somanath Salve Bhumika Chavan Rutuja. "A Review on Formulation and Evaluation of Effervescent Tablet." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 4428–38. https://doi.org/10.5281/zenodo.15521939.

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Although there are certain drawbacks to oral dosage forms compared to alternative approaches, such as the possibility of drug absorption, these can be addressed by providing the medicine in a liquid form, potentially enabling the use of lower dosages. Oral dosage forms are the most often used form of medication. However, many medications' volatility in liquid dose form limits their use. Creating effervescent tablets or granules, which are typically employed in quick-release arrangements, is an alternative to creating a dosage form that might hasten the dispersion and degradation of medications

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S., Aher Smita, Saudagar R. B., and Shinde Mayuri S. "REVIEW: FAST DISSOLVING TABLET." International Journal of Current Pharmaceutical Research 10, no. 2 (2018): 5. http://dx.doi.org/10.22159/ijcpr.2018v10i2.25876.

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Fast dissolving tablets is one of the most widely accepted dosage forms and also most popular dosage form, especially for pediatric patients because of incomplete development of the muscular and nervous system and a case of geriatric patients suffering from Parkinson’s disorder or hand tremors. Some solid dosage forms like tablets and capsules are present days facing the problems like difficulty in swallowing (dysphagia), resulting in many incidences of non-compliance and making the therapy ineffective. Oral dosage form and oral route are the most preferred route of administration for various

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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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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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Ahmed, Mohd Salman, Nikita Upadhyay, and P. K. Dubey. "A REVIEW ON FAST DISSOLVING TABLET." International Journal of Pharmaceutical Sciences and Medicine 7, no. 5 (2022): 37–47. http://dx.doi.org/10.47760/ijpsm.2022.v07i05.004.

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Fast dissolving tablets (FDTs) emerged as one of the popular and widely accepted dosage forms. Few solid dosage forms like capsules and tablets are present days facing the problems like difficulty in swallowing (dysphagia) resulting many incidences of non-compliance and making the therapy ineffective. Specifically for paediatric patients because of incomplete development of the muscular and nervous system and case of geriatric patients suffering from Parkinson’s disorder. Oral dosage form and oral route are the most preferred administration route for various drugs with limitations like first-p

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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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32

Agarwal, Shivendra, Raghvendra Misra, and Girendra Kumar Gautam. "FORMULATION, DEVELOPMENT AND IN VITRO EVALUATION OF TASTE MASKING MOUTH DISSOLVING TABLET OF LEVOCETIRIZINE DIHYDROCHLORIDE." International Journal of Pharma Professional’s Research (IJPPR) 14, no. 1 (2023): 47–58. http://dx.doi.org/10.48165/ijppronline.2023.14118.

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Levocetirizine dihydrochloride is a selective, long acting peripheral H1receptor antagonist. Allergic rhinitis is a symptomatic disorder of the nose induced by inflammation mediated by immunoglobulin E (IgE) in the membrane lining the nose after allergen exposure. Thus formulating Levocetirizine into an mouth dissolving tablet dosage form would provide fast relief. The Levocetirizine is bitter in taste so the Kyron T-114 (ion exchange resin) was used to mask the taste and to formulate an mouth dissolving tablet dosage form using drug resin complex. The tablets were evaluated for the drug conte

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Shejawal, Kanchan N., Anuja V. Chate, Yamini A. Sonar, and Prof Akanksha A. Suryawanshi. "The Incredible World of Tablet." International Journal for Research in Applied Science and Engineering Technology 11, no. 3 (2023): 231–38. http://dx.doi.org/10.22214/ijraset.2023.49399.

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Abstract: Pharmaceutical oral drug delivery is the most commonly used route of administration compared to other route of administration. Solid dosage forms are administered orally like tablets, capsules, pills, powders, etc. Tablet is the most widely used safest oral route of administration. Tablets are solid dosage form can be made directly from powders or from granules or from film coated multiple units. Tablets are also containing drug substances with or without diluents and prepared by compression or moulding methods. Tablets can be classified as compressed tablets and moulded tablets.

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Palwinder, Singh* and Rajeev Garg. "FAST DISSOLVING ORAL FILMS: A NOVEL TREND IN DOSAGE FORM." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 05 (2018): 4571–78. https://doi.org/10.5281/zenodo.1256824.

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Oral routes are most commonly preferred route for drug delivery. Commonly used oral dosage forms are tablet and capsules. But many patients such as geriatric, paediatric and dysphasic patients find difficulty in swallowing conventional tablet and capsule. To overcome the problems related to swallowing, Fast dissolving Tablets (FDTs) were designed in early 19th century and hence further advancement has led to development of Fast Dissolving Oral Films (FDOFs). Many pharmaceutical groups are focusing their research on rapid dissolving technology. FDOFs technology is gaining much attention. This t

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Patel, Salim G., and M. Siddaiah. "Formulation and evaluation of effervescent tablets: a review." Journal of Drug Delivery and Therapeutics 8, no. 6 (2018): 296–303. http://dx.doi.org/10.22270/jddt.v8i6.2021.

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Oral dosage forms are the most popular way of taking medication, despite having some disadvantages compared with other methods like risk of slow absorption of the medicament, which can be overcome by administering the drug in liquid form, therefore, possibly allowing the use of a lower dosage. However, instability of many drugs in liquid dosage form limits its use. Effervescent technique can be used as alternate to develop a dosage form which can accelerate drug disintegration and dissolution, is usually applied in quick release preparations. Along with the development of new pharmaceutical te

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S. Jabbar, Mohammed, and Yehia I. Khalil. "Formulation of Metoprolol Bilayer Tablets as an Oral Modified Release Dosage Form." Iraqi Journal of Pharmaceutical Sciences ( P-ISSN: 1683 - 3597 , E-ISSN : 2521 - 3512) 19, no. 1 (2017): 21–30. http://dx.doi.org/10.31351/vol19iss1pp21-30.

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Metoprolol is a Î²1 adrenergic blocker used in treatment of heart diseases. Metoprolol (100mg) tablets was formulated as a modified release oral system utilizing the concept of bilayer system, first layer contained (30mg) as immediate release and the other (70mg) in the sustained release matrix. The immediate release layer consisted of lactose or microcrystalline cellulose as diluents with sodium starch glycolate or sodium croscarmellose as disintegrants. The result showed that the layer contains microcrystalline cellulose and 2% sodium starch glycolate gave disintegration time similar to that

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Ganesh, M., C. V. Narasimharao, A. Saravana Kumar, et al. "UV Spectrophotometric Method for the Estimation of Valacyclovir HCl in Tablet Dosage Form." E-Journal of Chemistry 6, no. 3 (2009): 814–18. http://dx.doi.org/10.1155/2009/546187.

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A simple, sensitive, highly accurate UV spectrophotometric method has been developed for the determination of valacyclovir in bulk and tablet dosage form. Solution of valacyclovir in 0.1N HCl shows maximum absorbance at 255 nm. Beer’s law was obeyed in the concentration range of 5-25 mcg mL-1with 1.0910x104mol-1cm-1, the slope, intercept, correlation coefficient, detection and quantitation limits were also calculated. The proposed method has been applied successfully for the analysis of the drug in pure and in its tablets dosage forms. Result of percentage recovery and placebo interference sho

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M T, Ranjitha, and C. N. Somashekhar. "PREPARATION AND EVALUATION OF MEFENAMIC ACID AND DICYCLOMINE HYDROCHLORIDE AS ORAL DISINTEGRATING TABLET BY DIRECT COMPRESSION METHOD." Journal of Pharmaceutical and Scientific Innovation 10, no. 4 (2021): 94–101. http://dx.doi.org/10.7897/2277-4572.104211.

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A new dosage form, Oral disintegrating tablets (ODT’s) as a replacement to conventional oral dosage forms. ODT’s are dosage forms they disintegrate in mouth offering various advantages such as better mouth feel, dose accuracy, improved stability and convenient dosing as compared to oral liquids. So, there is need to designed oral disintegrating tablet to release the medicaments with an enhanced rate. Mefenamic acid is an anti- inflammatory drug while Dicyclomine HCl is anti-cholinergic drug. The combination of Mefenamic acid & Dicyclomine HCl controls pain very effectively, also relaxes bo

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Rutuja, Kokane* Ankita Matere Tushar Bagul. "Formulation and Evaluation of Herbal Tablet Dosage Form as a Slimming Product." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 4490–500. https://doi.org/10.5281/zenodo.15524063.

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Java plum seed powder has gained attention for its potential in weight management due to its nutritional and pharmacological properties. Formulating it into a tablet dosage form offers a convenient and effective way to harness its slimming benefits. This study formulates and evaluates a herbal tablet dosage form using Java plum seed powder as a slimming product. The powder’s physical and chemical properties are characterized, and suitable excipient are selected. Powder’s pre-evaluation parameters are evaluated for angle of repose, bulk density, tapped density, compressibility index

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Susheel, JV, S. Malathi, and TK Ravi. "Analysis of ropinirole in tablet dosage form." Indian Journal of Pharmaceutical Sciences 69, no. 4 (2007): 589. http://dx.doi.org/10.4103/0250-474x.36955.

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Pramod, Prakash Ronge* Dr. A.D. Shinde. "A REVIEW ON –FORMULATION AND IN-VITRO EVALUATION OF ORODISPERSIBLE TABLETS." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES o6, no. 05 (2019): 10991–1000. https://doi.org/10.5281/zenodo.3234069.

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<em>Recent advances in novel drug delivery (NDDS) aims to enhance the safety and efficacy of drug molecule by formulating a convenient dosage form for ease of administration and to achieve better patient compliance.</em><em> Orodispersible tablet is advanced and convenient drug delivery system, now days acquiring the most widely accepted dosage form. The recent advance in NDDS aimed for the development of dosage forms convenient to manufacturing and administration, immediate release and increased bioavailability.</em> <em>Orally disintegrating tablets are solid dosage forms containing drug tha

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Majeed, Saad M., Mohammed K. Al-Shaheen, Radhwan Nidal Al-Zidan, and Sameer M. Mahmood. "Multiple Unite Pellet Systems (MUPS) as Drug Delivery model." Journal of Drug Delivery and Therapeutics 10, no. 6 (2020): 231–35. http://dx.doi.org/10.22270/jddt.v10i6.4389.

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Multiparticulate drug delivery systems are mainly oral dosage form, consist of small discrete units that exhibit different characteristics especially in release pattern and drug bioavailability. These systems are represented by granules, pellets, microspheres, microcapsules, and minitablets. Pellets offer high flexibility in the design, formulation, and development of oral dosage forms such as sachet, suspension, capsule, and tablet. Multiparticulate tablets manufactured by compaction of multiple unite pellets is one of the latest and, yet, challenging technologies. Multiparticulate tablets co

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Karandule, Akshay, Komal Madake, Rajeshwari Khairnar, and Rupali Tasgaonkar. "Tablet Binders." International Journal for Research in Applied Science and Engineering Technology 11, no. 1 (2023): 675–81. http://dx.doi.org/10.22214/ijraset.2023.48663.

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Abstract: The tablet formulation contains binders that increase the interparticulate bond power inside the tablet. Research and progress of novel accessories remains a priority for potential use as a binder in formulations tablet. Tablet binder or binding agent are the substances that are added either dry or in liquid form during wet granulation to form granules or to promote cohesive compacts for directly compressed tablets. E.g., starch, pregelatinized starch, PEG, sorbitol, and HPMC, etc. Tablet Binder and disintegrants have the opposite used in an oral solid formulation. Binder delay table

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Sekhara Rao, M. Chandra, R. Chenna Krishna Reddy, K. B. Chandra Sekhar, and Y. V. Rami Reddy. "Identification and Detection of Finasteride Polymorphs in Finasteride Tablets by FT-Raman Spectroscopy." Asian Journal of Chemistry 32, no. 8 (2020): 1865–68. http://dx.doi.org/10.14233/ajchem.2020.22665.

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A simple FT-Raman spectroscopic method was developed for identification of finasteride polymorph form in finished dosage form. Finasteride polymorph form I was used in the tablet preparation and the weight fraction of finasteride in tablet was only about 0.023. The method was successfully used to identify the polymorphic form of finasteride in tablet and also to detect up to a level of about 15% of the other polymorph of finasteride present in the solid dosage. The dosage form was characterized by different techniques i.e. powdered X-ray diffraction, infrared spectroscopy and Raman spectroscop

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Wibowo, Teguh Setiawan, Diah Indah Kumala Sari, and Sri Bintang Sahara Mahaputra Kusuma Negara. "Training and Assistance in Tablet Manufacturing and Tablet Quality Control." Jurnal Pengabdian Masyarakat Bestari 3, no. 1 (2024): 13–24. http://dx.doi.org/10.55927/jpmb.v3i1.6854.

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Giving drug to patients or people who have been diagnosed with a disease is very rarely given as a pure active ingredient so most drugs are given in a dosage form. One form of drug dosage preferred by adult patients is a solid dosage form in the form of tablet. The aim is to increase understanding and technical abilities of pharmacy students in tablet manufacturing and tablet quality control. The method used was theoretical, practical and final evaluation which was carried out on 18 pharmacy students in the Pharmaceutical Technology Laboratory on the Universitas Muhammadiyah Lamongan. The resu

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Sa'adah, Hayatus. "OPTIMASI FORMULA EKSTRAK JAHE MERAH (Zingiber officinale) DENGAN METODE KEMPA LANGSUNG MENGGUNAKAN ANALISIS SIMPLEX LATTICE DESIGN." Jurnal Ilmiah Manuntung 1, no. 1 (2017): 47. http://dx.doi.org/10.51352/jim.v1i1.11.

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Processing of medicinal plants into the appropriate dosage form can ensure security during use. It is a motivation in making acceptable dosage form which is easy and convenient to use, especially the manufacture of ethanol extract red ginger tablets using a combination of starch 1500 and amprotab.The study begins with the manufacture of dry extract of red ginger. Optimization of making tablets using a combination of starch 1500 and disintegrator with simplex lattice design using three formulas is done by direct compaction method. Further testing on the tablet hardness, friability and disintegr

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Ms., Remya S. B., Subash Chandran M. P. Dr., and Aparna P. Ms. "Formulation and Evaluation of Cefixime Trihydrate Dispersible Tablets." International Journal of Trend in Scientific Research and Development 4, no. 1 (2019): 602–11. https://doi.org/10.5281/zenodo.3606058.

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Therapeutically active ingredients like tablet and capsule are conventional pharmaceutical dosage forms for manufacture, storage and ensure dosage uniformity. However, this dosage forms like capsules and tablets, often present ingestion problems such as difficulty in swallowing for the debilitated patients, particularly for paediatric and geriatric populations. This may result in a high incidence of non compliance and ineffective therapy, which may prove to be fatal in case of serious conditions. Suspension dosage forms could solve this problem, but they have other associated drawbacks like lo

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Rajeshwari Gokul Khairnar, Ashwini Ramdas Darade, and Rupali Rajesh Tasgaonkar. "A review on tablet binders as a pharmaceutical excipient." World Journal of Biology Pharmacy and Health Sciences 17, no. 3 (2024): 295–302. http://dx.doi.org/10.30574/wjbphs.2024.17.3.0142.

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The tablet formulation contains binders that increase the inter-particulate bond power inside the tablet. Research and progress of novel accessories remains a priority for potential use as a binder in formulations tablet. Tablet binder or binding agent are the substances that are added either dry or in liquid form during wet granulation to form granules or to promote cohesive compacts for directly compressed tablets. E.g., starch, pregelatinized starch, PEG, sorbitol, and HPMC, etc. Tablet Binder and disintegrants have the opposite used in an oral solid formulation. Binder delay tablet disinte

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Rajeshwari, Gokul Khairnar, Ramdas Darade Ashwini, and Rajesh Tasgaonkar Rupali. "A review on tablet binders as a pharmaceutical excipient." World Journal of Biology Pharmacy and Health Sciences 17, no. 3 (2024): 295–302. https://doi.org/10.5281/zenodo.11365349.

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The tablet formulation contains binders that increase the inter-particulate bond power inside the tablet. Research and progress of novel accessories remains a priority for potential use as a binder in formulations tablet. Tablet binder or binding agent are the substances that are added either dry or in liquid form during wet granulation to form granules or to promote cohesive compacts for directly compressed tablets. E.g., starch, pregelatinized starch, PEG, sorbitol, and HPMC, etc. Tablet Binder and disintegrants have the opposite used in an oral solid formulation. Binder delay tablet disinte

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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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