Relevant bibliographies by topics / Tablet Dosage Form

Contents

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

Academic literature on the topic 'Tablet Dosage Form'

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

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Tablet Dosage Form.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Tablet Dosage Form"

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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
6

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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
<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
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Tablet Dosage Form"

1

Lam, Matthew. "The making of liqui-pellet and liqui-tablet, the next generation oral dosage form." Thesis, University of Sussex, 2019. http://sro.sussex.ac.uk/id/eprint/81934/.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Bredenberg, Susanne. "New Concepts in Administration of Drugs in Tablet Form : Formulation and Evaluation of a Sublingual Tablet for Rapid Absorption, and Presentation of an Individualised Dose Administration System." Doctoral thesis, Uppsala University, Department of Pharmacy, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3433.

Full text
Abstract:
<p>This thesis presents two new concepts in oral drug administration and the results of evaluation of some relevant formulation factors.</p><p>Investigation into improving the homogeneity of mixtures for tableting indicated that it may be possible to obtain interactive dry mixtures of micronised drugs containing drug proportions as low as 0.015% w/w. By studying the relationship between disintegration time and tensile strength, it was found that the microstructure surrounding the disintegrant particles may influence the disintegration process. Therefore, avoidance of excipients which are highl
APA, Harvard, Vancouver, ISO, and other styles
3

Pavurala, Naresh. "Oral Drug Delivery -- Molecular Design and Transport Modeling." Diss., Virginia Tech, 2013. http://hdl.handle.net/10919/53505.

Full text
Abstract:
One of the major challenges faced by the pharmaceutical industry is to accelerate the product innovation process and reduce the time-to-market for new drug developments. This involves billions of dollars of investment due to the large amount of experimentation and validation processes involved. A computational modeling approach, which could explore the design space rapidly, reduce uncertainty and make better, faster and safer decisions, fits into the overall goal and complements the product development process. Our research focuses on the early preclinical stage of the drug development process
APA, Harvard, Vancouver, ISO, and other styles
4

Blair, Tina Caroline. "Some factors influencing the survival of microbial contamination in solid oral dosage forms." Thesis, King's College London (University of London), 1989. https://kclpure.kcl.ac.uk/portal/en/theses/some-factors-influencing-the-survival-of-microbial-contamination-in-solid-oral-dosage-forms(25307998-751d-4cb1-ae1b-49bf680e395c).html.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Patel, Fathima. "The development and assessment of a generic carbamazepine sustained release dosage form." Thesis, Rhodes University, 2006. http://eprints.ru.ac.za/1339/.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Munday, Dale Leslie. "Design, development and evaluation of encapsulated oral controlled release theophylline mini-tablets." Thesis, Rhodes University, 1991. http://hdl.handle.net/10962/d1003255.

Full text
Abstract:
Conventional solid dosage forms often lead to fluctuations which exceed the maximum safe therapeutic level and/or decline below the minimum effective level. It is recognised that many drugs for chronic administration should be administered on a schedule that maintains plasma drug concentration within the therapeutic window. Research in controlled release dosage forms aims at designing a system with a zero-order input (eg, ideally to deliver 8.33% of the dose per hour over a 12 hour duration), producing steady state plasma drug levels. Oral dministration of drugs prepared as a controlled releas
APA, Harvard, Vancouver, ISO, and other styles
7

Kieser, Leith Faye. "Formulation and assessment of monolithic beta blocker sustained release tablets prepared by direct compression." Thesis, Rhodes University, 2002. http://hdl.handle.net/10962/d1003242.

Full text
Abstract:
Beta blockers are commonly prescribed for the chronic treatment of hypertension, one of the most prolific disease states worldwide. The beta blockers selected for this study include acebutolol hydrochloride, labetalol hydrochloride, metoprolol tartrate oxprenolol hydrochloride and propranolol hydrochloride. All of these compounds have a short elimination half-life, necessitating multiple dose per day regimens and therefore the development of sustained release dosage forms incorporating these agents was considered beneficial in terms of extending the dosing interval, with the aim of improving p
APA, Harvard, Vancouver, ISO, and other styles
8

Kindgen, Sarah M. [Verfasser]. "Hydrodynamics and solid dosage form disintegration/dissolution : immediate release tablets and novel in situ polyelectrolyte gastroretentive drug delivery systems / Sarah M. Kindgen." Mainz : Universitätsbibliothek der Johannes Gutenberg-Universität Mainz, 2015. http://d-nb.info/1225749581/34.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Nobusa, Ana Lucia. "Desenvolvimento e avaliação de minicomprimidos de indapamida de liberação prolongada." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/9/9139/tde-08072011-104933/.

Full text
Abstract:
A hipertensão arterial é a principal causa da incidência de doenças cardiovasculares no mundo. Os diuréticos anti-hipertensivos como a indapamida são muito utilizados para o tratamento da hipertensão arterial, sendo a formulação de liberação prolongada muito eficaz e bem tolerada para o uso em pacientes idosos. Sistemas multiparticulados de formas farmacêuticas sólidas orais de liberação prolongada apresentam uma série de vantagens tecnológicas e biofarmacotécnicas em relação aos sistemas monolíticos.Assim, o presente trabalho teve como objetivo desenvolver formas farmacêutica sólidas multipar
APA, Harvard, Vancouver, ISO, and other styles
10

Mourão, Samanta Cardozo. "Correlação in vitro in vivo para formas farmacêuticas sólidas de liberação modificada contendo diclofenaco de sódio." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/9/9139/tde-06052010-095135/.

Full text
Abstract:
A correlação in vitro-in vivo (CIVIV) refere-se ao estabelecimento de uma relação racional entre as propriedades biológicas, ou parâmetros derivados destas, produzidos por uma forma farmacêutica e suas propriedades ou características físico-químicas. O estabelecimento desse tipo de correlação de dados pode possibilitar a substituição dos estudos in vivo, necessários à demonstração da bioequivalência, pelos estudos in vitro, no caso de alterações no processo de fabricação pós-registro. Os sistemas matriciais apresentam, como principal exemplo de material controlador da liberação, substâncias po
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Tablet Dosage Form"

1

1920-, Lieberman Herbert A., Lachman Leon 1929-, and Schwartz Joseph B. 1941-, eds. Pharmaceutical dosage forms--tablets. 2nd ed. Dekker, 1989.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Qiu, Yihong, Yisheng Chen, and Geoff G. Z. Zhang. Developing solid oral dosage forms: Pharmaceutical theory and practice. Edited by ScienceDirect (Online service). Academic, 2009.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

G, Brittain H., ed. Physical characterization of pharmaceutical solids. M. Dekker, 1995.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Shargel, Leon. Generic drug product development. CRC, 2007.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Isadore, Kanfer, and Shargel Leon 1941-, eds. Generic drug product development: Bioequivalence issues. Informa Healthcare, 2008.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Rp-Hplc Stability Indicating Assay and Simultaneous Estimation Method for the Combination of Glecapravir and Pibrentasvir in Tablet Dosage Form. Independently Published, 2020.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

(Editor), Herbert Lieberman, Leon Lachman (Editor), and Joseph B. Schwartz (Editor), eds. Pharmaceutical Dosage Forms: Tablets, Vol. 3 (Pharmaceutical Dosage Forms-Tablets). 2nd ed. Informa Healthcare, 1990.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

(Editor), Herbert Lieberman, Leon Lachman (Editor), and Joseph B. Schwartz (Editor), eds. Pharmaceutical Dosage Forms: Tablets, Vol. 2 (Pharmaceutical Dosage Forms-Tablets). 2nd ed. Informa Healthcare, 1990.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Pharmaceutical dosage forms: Tablets. 2nd ed. Dekker, 1990.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

Pharmaceutical Dosage Forms - Tablets. CRC Press LLC, 2008.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Tablet Dosage Form"

1

Subramanian, Muthukumar, Chellam Sankar, Gayathri Rajaram, and Vinesha Ravi. "Layered Tablets: A Novel Oral Solid Dosage Form." In Dosage Forms [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.108702.

Full text
Abstract:
Oral solid dosage forms hold a predominant position in the drug delivery system. Tablets are the most widely used and convenient dosage form. Due to their ease of manufacturing, the minimum cost of production, easy handling and storage, and better stability, tablets are most preferred. Patients who are prescribed more than one drug are in a situation to consume multiple tablets. To minimize the counts, one or more drugs are cast into layers to form a single tablet, thus called layered tablets. Layered tablets tend to improve patient compliance and reduce the cost of production by half. Layers
APA, Harvard, Vancouver, ISO, and other styles
2

Dahlöf, Carl G. H. "Characteristics of different routes of administration." In The Triptans: Novel Drugs for Migraine. Oxford University PressNew York, NY, 2001. http://dx.doi.org/10.1093/oso/9780192632142.003.0010.

Full text
Abstract:
Abstract The availability of several triptan formulations provides an opportunity to tailor therapy to individual patients’ needs. For the majority of patients, tablets, which offer more or less consistent efficacy within 30 min of administration in a convenient dosing form, may be an appropriate choice. Although clinical trials do not demonstrate robust differences in efficacy between triptan tablets, individual patients do distinguish them and often have a preference for one triptan or dose over another. For those having difficulties in swallowing a tablet, the freeze-dried fast-melting tabl
APA, Harvard, Vancouver, ISO, and other styles
3

Shah, Rutuja R., Swapnil S. Patil, and PoonamJ aykar Patil. "PHARMACEUTICAL PREPARATIONS AND DRUG DELIVERY." In Futuristic Trends in Pharmacy & Nursing Volume 3 Book 5. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bapn5ch25.

Full text
Abstract:
In present chapter we have focused on different pharmaceutical dosage form and classified them on basis of their physical appearance and route of administration as well.Objectives of converting drug in to dosage form and there merits are highlighted.AProaches of formulating different dosage form and there stability is focused in current chapter.Development of pharmaceutical dosage form is art and science of inventing new dosage form by Pharmacists and pharmaceutical scientists.In this chapter we are going to introduce different concepts related to pharmaceutical prepartions and drug delivery.
APA, Harvard, Vancouver, ISO, and other styles
4

Sowmyasree, Golla Venkata. "Tablets." In A Text Book of Pharmaceutics for I Year Diploma in Pharmacy. THINKPLUS PHARMA PUBLICATIONS, 2024. http://dx.doi.org/10.69613/736rs621.

Full text
Abstract:
Tablets are the most widely used solid dosage form in pharmaceutical practice, offering advantages such as precise dosing, stability, and patient convenience. This section explores the various types of tablets, including immediate-release, modified-release, and orally disintegrating tablets, each designed to meet specific therapeutic needs. The composition of tablets, including active ingredients and excipients such as diluents, binders, disintegrants, and lubricants, is discussed in detail. Tablet manufacturing processes, from wet granulation and dry granulation to direct compression, are exa
APA, Harvard, Vancouver, ISO, and other styles
5

Mohammed, Jahasultana, Narender Malothu, Narayana Murthy Ganta, Nestory Mbilinyi, J. Uma Maheswari, and Monzir Idris. "A UV-Spectrophotometric Method for Simultaneous Estimation of Abacavir and Lamivudine in their Pharmaceutical Dosage Forms." In Current Trends in Drug Discovery, Development and Delivery (CTD4-2022). Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/9781837671090-00220.

Full text
Abstract:
The combination of Abacavir (ABA) and lamivudine (LAM) is being used in the treatment of HIV. Though, there was several spectroscopic methods have been reported, it needs a simple, sensitive, and rapid analytical method for precise analysis. The objective of the current research was to establish a UV-spectrophotometric method for simultaneous estimation of in their bulk and tablet dosage form. In the current study, both drugs were estimated by simultaneous equation method. The method is characterized by measurement of absorbances at two wavelengths 218 nm and 274 nm, λmax of ABA and LAM, respe
APA, Harvard, Vancouver, ISO, and other styles
6

VADAGA, ANILKUMAR. "Pharmaceutical Aids." In A Text Book of Pharmaceutics for I Year Diploma in Pharmacy. THINKPLUS PHARMA PUBLICATIONS, 2024. http://dx.doi.org/10.69613/5zhfxq55.

Full text
Abstract:
Pharmaceutical aids, also known as excipients, are essential components in drug formulations that serve various functions beyond the active pharmaceutical ingredient (API). These substances play crucial roles in enhancing the stability, bioavailability, manufacturability, and patient acceptability of medicinal products. Common categories of pharmaceutical aids include diluents, binders, disintegrants, lubricants, glidants, and preservatives. Each type of excipient contributes uniquely to the overall performance of the dosage form. For instance, diluents provide bulk to small-dose drugs, while
APA, Harvard, Vancouver, ISO, and other styles
7

Khan, Amjad, Shabnam Nazir, Hamad S. Alyami, and Aman Ullah. "SeDeM-ODT Expert System: A Solution to Challenges in Characterization of Pharmaceutical Powders and Powdered Material." In Advanced Functional Materials. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.92444.

Full text
Abstract:
In the field of pharmaceutical sciences, material characterization has been a focus of research as properties of the powder ingredients govern characteristics of the finished dosage form. It has been a tedious and time-consuming job to develop a correlation between the characteristics of powder material and final dosage form. Extensive experimentation is carried out at different stages of formulation development to optimize the final blend and produce a product fulfilling official requirements. Various approaches have been applied for the purpose with varying degree of applications. SeDeM-ODT
APA, Harvard, Vancouver, ISO, and other styles
8

Kaur, Navneet, Rajip Nepal, and Surg Lt Cdr (Dr) Prabhjot Singh. "INTRODUCTION TO BIOPHARMACEUTICS." In Futuristic Trends in Pharmacy & Nursing Volume 2 Book 24. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2023. http://dx.doi.org/10.58532/v2bs24ch4.

Full text
Abstract:
Biopharmaceutics is the relationship among drug’s all properties like organolaptic properties, hydrolysis, oxidation, reduction, racemization etc, and its dosage formulation, also administration route. The sequence of events that predict elicitation, therapeutic effect of drug are important as a drug in its form and formulation of drug on the absorption and distribution to the target site. Initially the drug is absorbed orally or by any other route followed by release in predictable manner after that some portion of drug reaches to surrounding tissues finally reaches to the target site. Now we
APA, Harvard, Vancouver, ISO, and other styles
9

Gopal, N. Madana, L. Siva Sanker Reddy, and R. Nageswara Rao. "METHOD DEVELOPMENT AND VALIDATION OF CILNIDIPINE IN TABLET DOSAGE FORM BY USING ULTRA VIOLET SPECTROPHOTOMETRY." In Futuristic Trends in Pharmacy & Nursing Volume 3 Book 11. Iterative International Publisher, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bgpn11p2ch5.

Full text
Abstract:
A simple, quick, and accurate UV Spectroscopic method was developed to quantify celecoxib in API and tablet formulations. Celecoxib was used to treat rheumatoid arthritis and osteoarthritis. The proposed procedure was developed using acetonitrile and distilled water as the solvents in a 50:50 volume-to-volume ratio, and it was optimized using a Shimadzu UV-1800 ENG240V at a maximum wavelength of 240 nm with an absorbance of 0.558. The sensitivity, robustness, accuracy, and precision of the improved technique Degradation studies were also conducted and determined to be within the constraints. T
APA, Harvard, Vancouver, ISO, and other styles
10

Satapathy, Bhagyalata, and Chaitanya Bangari. "Estimation of Ribociclib and Letrozole in Solid Dosage form (Tablet): A Novel Analytical Method." In Current Overview on Pharmaceutical Science Vol. 9. B P International (a part of SCIENCEDOMAIN International), 2023. http://dx.doi.org/10.9734/bpi/cops/v9/3713b.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Tablet Dosage Form"

1

Sibychan, Jerrin Job, Nicola Sorace, Jason Melnick, et al. "Use of Discrete Element Method to Troubleshoot Aesthetic Defects in Pharmaceutical Tablets." In Foundations of Computer-Aided Process Design. PSE Press, 2024. http://dx.doi.org/10.69997/sct.148066.

Full text
Abstract:
Pharmaceutically elegant tablets are an expectation from pharmacists, health care providers and consumers for solid oral dosage forms. The presence of non-aesthetically pleasing defects in solid oral dosage forms can result in complaints back to the manufacturer and potentially non-compliance with medicines. The purpose of this study was to simulate and analyze the design of a tablet core and the aqueous film-coating process, to gain a better understanding of tablet defect generation, and to help eliminate the defects from the finished product. This evaluation employs Discrete Element Method (
APA, Harvard, Vancouver, ISO, and other styles
2

Shahab, Mohammad, Kensaku Matsunami, Zoltan Nagy, and Gintaras Reklaitis. "Process analysis of end-to-end continuous pharmaceutical manufacturing using PharmaPy." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.154363.

Full text
Abstract:
As pharmaceutical manufacturing is transitioning from traditional batch to continuous manufacturing (CM), there is a lack of tools for CM design and development, which can integrate drug substance and drug product unit operations for overall evaluation. Recently, a Python-based PharmaPy framework was proposed to advance the design, simulation, and analysis of continuous pharmaceutical processes. However, the initial library of models only addressed upstream drug substance processing. In this work, new capabilities, including drug product unit operations such as feeder, blender, and tablet pres
APA, Harvard, Vancouver, ISO, and other styles
3

Ganzer, G. A., M. Freid, J. Summerfield, J. Soost, and G. Reggiani. "The Use of a Glutaraldehyde/DBNPA Combination Treatment Program for Effective Control of Microbial Growth in Cooling Water Systems." In CORROSION 2002. NACE International, 2002. https://doi.org/10.5006/c2002-02005.

Full text
Abstract:
Abstract Combination biocide products are finding increased use in cooling water systems as an effective means of providing consistent microbial control under a wide variety of conditions. The use of two biocides gives broader spectrum control than using one product alone and also limits the potential of tolerance development with one treatment active. Optimum protection can be achieved when one biocide is applied continuously and the other intermittently. An effective biocide combination is glutaraldehyde, fed on a slug dose basis, concurrent with a low level continuous use of DBNPA, convenie
APA, Harvard, Vancouver, ISO, and other styles
4

Balawajder, Peter, Jeffrey Steward, Alfonso Ortega, Joe D’Silva, Anne Moore, and Luis Silva. "Investigation of a Novel Process for Wet Milling a Pharmaceutical Tablet in a Dynamically Rotating Water-Filled Dosage Cup." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-10669.

Full text
Abstract:
The most common commercial pharmaceutical dosage forms are tablets and capsules, but unfortunately these forms may not be suitable for sub-groups, such as very ill children and elderly patients and those experiencing trauma and involved in surgery. Many of these patients have difficulty in swallowing a solid dosage form. For these groups, the general practice is to use equipment such as the age-old mortar and pestle to pulverize the tablet, transfer the powder to a container and then make a liquid suspension by addition of water. This process consists of two unit processes: dry grinding follow
APA, Harvard, Vancouver, ISO, and other styles
5

Благоразумная, Наталья Васильевна, Дарья Сергеевна Волокитина, and Людмила Николаевна Дуккардт. "IDENTIFICATION OF ALLOPURINOL IN MILD DOSAGE FORM FOR THE TREATMENT OF HYPERURICEMIA." In Современные методы и инновации в науке: сборник статей XL международной научной конференции (Санкт-Петербург, Декабрь 2024). Crossref, 2025. https://doi.org/10.37539/241209.2024.62.47.002.

Full text
Abstract:
Заболевания, связанные с нарушением выведения почками мочевой кислоты и приводящие, в связи с этим к образованию мочевых конкрементов, довольно широко распространены у лиц старше 40 лет. К этим заболевания относится подагра. К числу средств, применяемых при лечении подагры, относятся препараты, уменьшающие содержание мочевой кислоты в крови - относится аллопуринол (милурит). В настоящее время это лекарственное средство выпускается в форме таблеток. Учитывая высокие биофармацевтические характеристики гелей, как современной лекарственной формы, нами предпринята попытка разработать гель с аллопур
APA, Harvard, Vancouver, ISO, and other styles
6

Akram, N. MD, N. Madana Gopal, A. Balakrishna, N. Bakthavatchala Reddy, G. Sravya, and Grigory V. Zyryanov. "RP-HPLC method for the simultaneous analysis of ambroxol hydrochloride and nitazoxanide in API and tablet dosage form." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0070416.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Tarigan, Rida Evalina, Muchlisyam, Siti Morin Sinaga, and Zul Alfian. "Development and validation of area under curve spectrophotometry method for ternary mixture of dextromethorphan HBr, doxylamine succinate and pseudoephedrine HCl in tablet dosage form." In THE INTERNATIONAL CONFERENCE ON CHEMICAL SCIENCE AND TECHNOLOGY (ICCST – 2020): Chemical Science and Technology Innovation for a Better Future. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0045551.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Akseki, Ilgaz, Christopher F. Libordi, and Cetin Cetinkaya. "Non-Contact Acoustic Techniques for Drug Tablet Monitoring." In ASME 2006 International Mechanical Engineering Congress and Exposition. ASMEDC, 2006. http://dx.doi.org/10.1115/imece2006-13940.

Full text
Abstract:
Quality assurance monitoring and material characterization is of great importance in the pharmaceutical industry. If the tablet coating and/or core are defective, the desired dose delivery and bioavailability can be compromised. Tablet coatings serve a wide variety of purposes such as regulating controlled release of active ingredients in the body, contributing to the bioavailability of a particular drug or combination of drugs, during certain times and locations within the body, protecting the stomach from high concentrations of active ingredients, extending the shelf life by protecting the i
APA, Harvard, Vancouver, ISO, and other styles
9

Yang, Li, Xinpeng Li, Yixue Chen, Boxin Wang, and Sheng Fang. "Optimization for Rapid Dose Calculation of the RIMPUFF Model and Its Evaluation Against Belgian Field Experiment." In 2022 29th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/icone29-90806.

Full text
Abstract:
Abstract The Risø Mesoscale PUFF model (RIMPUFF) is a Lagrangian atmospheric dispersion model that uses consecutive Gaussian puffs to simulate accidental release which is widely used in nuclear emergencies. Based on the real-time puff size and the distance between the puff and the monitoring station, RIMPUFF can calculate the dose results quickly by using the dose calculation interpolation table within its dose calculation module but the results are biased. To improve the accuracy of dose results under the requirement of rapid dose calculation, in this paper, a new interpolation table for dose
APA, Harvard, Vancouver, ISO, and other styles
10

Kaushik, Sandipan, Mohammed Sonebi, Giuseppina Amato, Arnaud Perrot, and Utpal Kumar Das. "Effect of Mix Proportions on Fresh and Rheological Properties of Cementitious Mixture Containing Natural Fibre: Modelling Using Factorial Design." In 4th International Conference on Bio-Based Building Materials. Trans Tech Publications Ltd, 2022. http://dx.doi.org/10.4028/www.scientific.net/cta.1.309.

Full text
Abstract:
This paper aims to discuss the influence of mix composition of cement mortar on fresh and rheological properties of cement mortar. Two different natural fibres, basalt (BA) and sisal (SL) are selected based on fresh and rheological behaviour for its usability in a cementitious mixture. The workability and rheological behaviour are evaluated by flow table test, cone penetrometer and slump test of the mixture. A full factorial design method was used to investigate the effects of four mix components: dosage of cement content (B), percentage of fly-ash (FA) by mass of cement, dosage of basalt fibr
APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Tablet Dosage Form"

1

Puthanakit, Thanyawee, Kiat Ruxrungtham, Chitsanu Pancharoen, Jintanat Ananworanich, Torsak Burunupradah, and Arunee Klinklom. Pharmacokinetics of low-dose lopinavir/ritonavir tablet formulation in HIV-1 infected children. Chulalongkorn University, 2010. https://doi.org/10.58837/chula.res.2010.14.

Full text
Abstract:
Methods: This was an open-label, cross-over study of 24 HIV-infected children with HIV RNA &lt; 50 copies/ml comparing PK parameter of standard dose LPV/r and low dose of LPV/r for 4 weeks. LPV dosage was prescribed by body weight band; 25~35 kg: LPV/r 300/75 vs. 200/50 mg, &gt; 35 kg 400/100 vs. 300/75 mg. Glood samples were drawn at 0 (pre-dose), 2,4,6,8, 10 and 12 hours. Plasma concentrations of LPV and RTV were measured by HPLC method. The acceptable C12h is &gt; 1 mg/L. The HIV RNA was measured at week 12 after switch back to standard dose for 4 weeks. Results: Twenty four children were i
APA, Harvard, Vancouver, ISO, and other styles
2

Lichter, Amnon, Joseph L. Smilanick, Dennis A. Margosan, and Susan Lurie. Ethanol for postharvest decay control of table grapes: application and mode of action. United States Department of Agriculture, 2005. http://dx.doi.org/10.32747/2005.7587217.bard.

Full text
Abstract:
Original objectives: Dipping of table grapes in ethanol was determined to be an effective measure to control postharvest gray mold infection caused by Botrytis cinerea. Our objectives were to study the effects of ethanol on B.cinerea and table grapes and to conduct research that will facilitate the implementation of this treatment. Background: Botrytis cinerea is known as the major pathogen of table grapes in cold storage. To date, the only commercial technology to control it relied on sulfur dioxide (SO₂) implemented by either fumigation of storage facilities or from slow release generator pa
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Tablet Dosage Form' for particular source types:
Journal articles Dissertations / Theses Books
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography