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Journal articles on the topic 'Tablet Evaluation'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

Treesinchai, Sakonjan, Satit Puttipipatkhachorn, Tasana Pitaksuteepong, and Srisagul Sungthongjeen. "Evaluation of Curcuminoids Effervescent Floating Tablets." Advanced Materials Research 1060 (December 2014): 25–28. http://dx.doi.org/10.4028/www.scientific.net/amr.1060.25.

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The objective of this study was to develop and evaluate curcuminoids effervescent floating tablet. The system consists of a curcuminoids-containing core tablet coated with a gas forming layer (tartaric acid layer and sodium bicarbonate layer divided by a protective layer (hydroxypropyl methylcellulose)) and a gas-entrapped membrane (Eudragit® RL 30D), respectively. The floating tablets using lactose as a filler showed higher drug release than those using microcrystalline cellulose (MCC) or MCC:lactose as a filler. However, type of core tablet fillers did not affect time to float of the floatin

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Gawande, Siddhant, Aditya Ghadge, and Asmita Sakore. "Expression and Evaluation of Polyherbal Tablet." International Journal of Pharmaceutical Research and Applications 09, no. 06 (2024): 797–803. https://doi.org/10.35629/4494-0906797803.

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Herbal tablet expression dates back to ancient civilisations, where traditional knowledge and natural resources were employed to create effective remedies. They used a combination of powdered plant substance, natural binders and manual compression techniques to formulate the tablets. Historical records from regions similar as India, China, and the Mediterranean reveal different approaches to herbal tablet preparation. Herbal tablet surfaced as a safe, effective, and accessible substitute to synthetic medicine. This study focuses on the expression and evaluation of a herbal tablet prepared usin

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Dipali, Kakade1 Shabnam khan2 Ramakant Sharma2 Jeevan Patel2 Shivani Khoware2 Rakesh Patel3. "Formulation and Evaluation of Montelukast levocetirizine Tablet." International Journal in Pharmaceutical Sciences 2, no. 3 (2024): 182–92. https://doi.org/10.5281/zenodo.10794492.

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Formulation and Evaluation of tablet containing combination of Montelukast and    Levocetirizine. The objective of present work is-To improve and increase the stability of both montelukast and Levocetirizine in combination as tablet. Enhancement of dissolution of Montelukast. To formulate and evaluate tablets of Levocetirizine and Montelukast for treating allergic rhinitis effectively. The begin with general introduction presenting overview about drugs for allergic rhinitis and combination of montelukast and Levocetirizine tablet. In the present research work, montelukast Levoce

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Bharat, Jadhav* Rutuja Dhas Sahil T. Shaikh. "EVALUATION OF THE GENERAL MARKETED TABLET." International Journal in Pharmaceutical Sciences 2, no. 2 (2024): 176–83. https://doi.org/10.5281/zenodo.10629019.

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The evaluation of diclofenac potassium tablets involved rigorous testing to ensure quality and efficacy. Tests included hardness assessment to gauge tablet strength, friability testing to determine resistance to action analysis was conducted to ensure uniformity among tablets. This comprehensive evaabrasion, and disintegration tests to assess dissolution properties. Additionally, weight evaluation provides valuable insights into the tablets' physical characteristics, aiding in the assurance of product quality and consistency. This study focuses on the comprehensive evaluation of diclofenac pot

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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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Rajni, Dubey1 Saniya Mubarik*2 Bhaskar Kumar Gupta3 Mariya Beg1. "Formulation and Evaluation of By-Layered Tablet." International Journal of Pharmaceutical Sciences 3, no. 3 (2025): 2848–95. https://doi.org/10.5281/zenodo.15101573.

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Several pharmaceutical companies are currently developing bi- layer tablets for a variety of reasons like patent extension, therapeutic efficacy, marketing etc. This technology has been used to reduce capital investment. Modified tablet presses have been used to develop bilayer tablets in order to overcome problems associated with tablets like layer separation, insufficient hardness, inaccurate individual layer weight control, cross contamination between the layers, reduce yield etc. When high production output is required a modified tablet, press is used.

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7

Akhtar, Sabina, and Pulak Dev. "FORMULATION AND EVALUATION OF CHEWABLE MULTIVITAMIN TABLET." International Journal of Current Pharmaceutical Research 9, no. 4 (2017): 61. http://dx.doi.org/10.22159/ijcpr.2017v9i4.20958.

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Objective: The overall objective of the present study was to formulate the chewable multivitamin tablet prepared by direct compression method.Methods: The excipient used in this study are mannitol, sucrose, starch, talc, magnesium stearate, vanilla powder for the effective formulation. As it is multivitamin, ascorbic acid, riboflavin, nicotinamide, thiamine HCL are used and evaluated for precompression parameter. The chewable tablets were better presented using sweetener sucrose and vanilla powder as a flavouring agent. The formulated tablet was evaluated for post compression parameter. The ch

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Sonare, Makrand A., and Manoj Kumar Samantaray. "Pharmaceutical evaluation of Haridra Khanda tablet." Journal of Ayurveda and Integrated Medical Sciences (JAIMS) 5, no. 05 (2020): 175–78. http://dx.doi.org/10.21760/jaims.5.5.24.

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Haridra Khanda is unique classical formulation indicated in Udarda, Shitapitta, Kotha. (Urticarial rashes) Khanda or Granules are a comparatively unusual means of administering drugs that possess an unpleasant taste. Haridra Khanda is classical Ayurvedic medicine and available market. Keeping the issue of palatability and invention of patient friendly dosage form in mind, the efforts was made for preparation of tablet out of classical Ayurvedic formulation - Haridra Khanda. The preparation of Haridra Khanda granules were made by standard operative procedure.Binding agents were added to Haridra

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9

Haryono, Ika Avrilina, and Noval Noval. "Formulasi dan Evaluasi Tablet Effervescent dari Ekstrak Buah Tampoi (Baccaurea macrocarpa)." Jurnal Surya Medika 7, no. 2 (2022): 34–44. http://dx.doi.org/10.33084/jsm.v7i2.3201.

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Tampoi is one of the many plants found in East Kalimantan, has secondary metabolic content in the form of saponins, flavonoids, and alkaloids, and has antioxidant activity. The antioxidants produced by the human body are not sufficient to fight free radicals, therefore the body requires the intake of antioxidants from the outside, so to help increase public interest in consumption, researchers are interested in making preparations in the form of extracts and formulated as effervescent tablets from tampoi fruit extract which are useful as antioxidants and increase immunity. The purpose of this

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Journal, Devanshi, Dibya Kumari, and Umesh Kumar Jain. "Formulation and Evaluation of Gastroretentive Bilayer Tablets." Journal of Drug Delivery and Therapeutics 14, no. 9 (2024): 107–12. http://dx.doi.org/10.22270/jddt.v14i9.6784.

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Gastroretentive bilayer tablets were designed to prolong the gastric residence time after oral administration and to achieve immediate release of lansoprazole and controlled release floating layer of clarithromycin to treat gastric ulcers. Instant release layer has a combination of super disintegrating agents. A combination of effervescent mechanism is used. HPMC K5 was used as swelling polymer and citric acid, sodium bicarbonate as gas generating agent to reduce the floating lag time. Bilayer floating tablets were prepared with varying proportions of instant layer and sustained release floati

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11

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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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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13

Balcha Balla, Tamrat, Nisha MaryJoseph, and Anteneh Belete. "In Vitro Evaluation of Native Taro Boloso-I Starch as a Disintegrant in Tablet Formulations." Advances in Materials Science and Engineering 2021 (December 24, 2021): 1–10. http://dx.doi.org/10.1155/2021/7576730.

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Introduction. In drug delivery, solid dosage forms, of which tablet is the commonest, are still the leading preferences. An area of research focus in tablet drug delivery is the search for tablet excipients. This study was aimed at evaluating and optimizing native Taro Boloso-I starch as a tablet disintegrant. Methods. The response surface method with central composite design (CCD-RSM) was used for the analysis and optimization of the concentration of native Taro Boloso-I starch and compression force. Wet granulation method was used for the preparation of paracetamol tablets. The response vari

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14

Swetanshu, ,., and Vijay Sharma. "Formulation, Optimization and Evaluation of Bilayer Tablet of Antihypertensive Drug." Journal of Drug Delivery and Therapeutics 9, no. 4 (2019): 704–8. http://dx.doi.org/10.22270/jddt.v9i4.3098.

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Hypertension or high blood pressure occurs when the high cardiac output exerts pressure on the arterial wall as the blood flow increases. Bi-layer tablets are prepared with one layer of drug for immediate release while second layer designed to release drug later, either as second dose or in an extended release manner. Bi-layered tablet is suitable for sequential release of two drugs in combination, separate two incompatible substances, and also for sustained release tablet in which one layer is immediate release as initial dose and second layer is maintenance dose. Bilayer tablet is suitable f

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15

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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16

Khan, MD Abdul Aali, M. S. Sudheesh, and Rajesh Singh Pawar. "Formulation Development and Evaluation of Oro-Dispersible Tablets Based On Solid Dispersion of Cimetidine." Journal of Drug Delivery and Therapeutics 12, no. 6-S (2022): 42–46. http://dx.doi.org/10.22270/jddt.v12i6-s.5696.

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The most common problem about conventional dosage form is dysphagia (difficulty in swallowing). So, we design a new approach in a conventional dosage form which is oral dispersible tablet. Oral dispersible tablet is also called as mouth dissolving tablet, fast dissolving tablet, or oral disintegrating tablet. Oral dispersible tablet has advantage as it quickly disintegrates into saliva when it is put on the tongue. The faster the drug disintegrates or is dissolved, the faster the absorption and the quicker the therapeutic effect of drug will be attained. The objective of present study was to f

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17

Socorrina, Colaco Ramesh. N. Ramakrishna Shabaraya. "FORMULAITON AND PHARMACOKINETIC EVALUATION OF NAPROXEN SODIUM MODIFIED RELEASE TABLET." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 05 (2018): 3960–67. https://doi.org/10.5281/zenodo.1249923.

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The objective of the study was to develop naproxen sodium SR tablets were prepared by direct compression method using hydroxy propyl methyl cellulose (HPMC K 100). To know the effect of polymer concentration invitro study performed it has been observed that as the polymer concentration increases, the drug release rate decreases, and bioavailability study carried out in healthy human subject by administering the developed sustained release and marketed immediate release tablet. The developed naproxen sodium showed confirmed longer time to reach peak concentration than marketed immediate release

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18

Karima, Nurul. "Formulation and Evaluation of Solid Dispersion Griseofulvin Tablets." Indonesian Journal of Science and Pharmacy 2, no. 1 (2024): 6–9. https://doi.org/10.63763/ijsp.v2i1.60.

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Griseofulvin is one of the systemic treatments for the treatment of dermatophytes found on the skin, scalp and nails. Griseofulvin is a BCS class II group that has low solubility and high permeability. Increasing solubility is one of them by using a solid dispersion system. In this study, the solid dispersion obtained was formulated in tablet form. The purpose of this study was to increase the solubility of griseofulvin. The method used was experimental, solid dispersion using PEG 6000 as a carrier, with XRD, SEM, and FTIR test parameters. Furthermore, the solid dispersion obtained was formula

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19

Mr.SMahendran, Mr SMahendran, Mrs Sreya KR Mrs.Sreya KR, Fathima RinshaC Fathima RinshaC, et al. "Formulation and evaluation of chewable Toothpaste Tablets." International Journal of Pharmaceutical Research and Applications 10, no. 2 (2025): 1352–57. https://doi.org/10.35629/4494-100213521357.

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In this study, we present the Formulation and Evaluation of Chewable Toothpaste Tablets as a sustainable alternative to conventional toothpaste. Chewable toothpaste tablets are an innovative alternative to traditional toothpaste, offering portability, convenience, and environmental sustainability by eliminating the need for plastic tubes. This project focuses on the formulation and evaluation of chewable toothpaste tablets designed to provide effective oral hygiene. This formulation incorporates key ingredients such as strawberry and xylitol for cavity prevention, calcium carbonate as an abras

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20

Masih, Ashish, and Ajay Kumar Tiwari. "FORMULATION AND EVALUATION OF FAST DISSOLVING TABLETS OF AMOXYCILLIN TRIHYDRATE AND POTASSIUM CLAVULANATE." International Journal of Current Pharmaceutical Research 9, no. 2 (2017): 48. http://dx.doi.org/10.22159/ijcpr.2017v9i2.17385.

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Objective: The present work is aimed to formulate fast dissolving stable tablet formulation a preferred combination of Amoxycillin trihydrate (Beta-lactum antibiotic) and Potassium clavulanate (Beta-lactum inhibitor) by using various super disintegrants.Methods: Fast dissolving tablets are prepared by direct compression method using super disintegrants i.e. sodium starch glycolate, crospovidone, croscarmellose sodium. Aspartame as a sweetener and trusil mango flavor were used to increase palatability. Reduction in the dose of Amoxycillin trihydrate and Potassium clavulanate tablet was possible

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Sahasrabuddhe, Vishakha, M. Alagusundaram, Vijeta Bhattacharya, Namrata Mishra, and Priyanka Keshri. "Formulation and Evaluation of Ascorbic Acid Mouth Dissolving Tablets." Asian Journal of Basic Science & Research 06, no. 02 (2024): 167–82. http://dx.doi.org/10.38177/ajbsr.2024.6213.

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Mouth dissolving tablet have better accessibility and tolerability for patients, mouth dissolving tablet is the most essential and recommended way of drug delivery. One more difficulty can be solved by administering the new drug with the mouth dissolving tablet formulation so that the drug quickly dissolves and breaks in the mouth in fewer minute due to the effect of super disintegrating agents that maximize the pore structure of the formulation. The purpose of this research work was to develop mouth-dissolving tablet of Ascorbic Acid. Tablet containing drug and excipients were prepared by dir

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Ramesh, Pastham, Reddy Sunil, and Allenki Venkatesam. "Design and In-vitro Evaluation of Enteric Coated Pulsatile Drug Delivery System of Zileuton Tablets." Pharmaceutical and Chemical Journal 4, no. 4 (2017): 57–65. https://doi.org/10.5281/zenodo.13785001.

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In the present research work pulsatile drug delivery system of Zileuton tablets were formulated by employing compression coating technology. Initially the core tablets were prepared by 30% concentrations of super disintegrates, the formulated core tablets were coated with the polymers by using compression coating technology. All the core and press coated tablet formulations were subjected to various physical and chemical evaluation tests for core and press coated tablets. The thickness, hardness and weight variation shown by all the tablet formulations were found within the official pharmacopo

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23

Arpit Kumar, Arpit Kumar, Dr Suneel Kumar Niranjan, and Umesh Patel. "Formulation and Evaluation of Matrix dissolving Tablet of Isoniazid: Controlled Release." International Journal of Pharmaceutical Research and Applications 10, no. 3 (2025): 1641–45. https://doi.org/10.35629/4494-100316411645.

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Isoniazidis a cornerstone in the treatment of tuberculosis (TB), yet its conventional administrationis associated with challenges such as frequent dosing and potential hepatotoxicity. Matrix dissolving tablet formulations aim to address these issues by providing controlled drug release, enhancing patient compliance, and minimizing side effects. This review explores various formulation strategies, methodologies employed in developing matrix dissolving tablets of isoniazid, emphasizing the role of both natural and synthetic polymers in modulating drug release profiles. The review paper also cove

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Gandhi, Kunjan, Sunil Kumar Shah, C. K. Tyagi, Prabhakar Budholiya, and Harish Pandey. "Formulation, Development and Evaluation of Uncoated Bilayer Tablet of Anti-Hypertensive Agents." Journal of Drug Delivery and Therapeutics 10, no. 4-s (2020): 100–107. http://dx.doi.org/10.22270/jddt.v10i4-s.4229.

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The present research work was carried out to Formulate and evaluation of bilayer tablet dosage form for the treatment of Hypertension.The objective of this study to compare the specific characteristics of Metoprolol [beta selective (cardio selective) adrenoreceptor blocking agent] and Hydrochlorothiazide (Thiazide Diuretics]) in order to design stable formulation. It can be concluded that bilayer tablet were successfully formulated to achieve immediate release of Hydrochlorothiazide (HCTZ) and tailored release of Metoprolol (MPL)by using Dual Release Drug Absorption System(DUREDAS technology).

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Ermawati, Dian Eka, Rido Rohana Tambunan, and Ulfa Afrinurfadhilah Darojati. "The Effect of Combination of Porang Tuber Starch (Amorphophallus muelleri Blume) with Lactose on the Physical Properties of Bajakah Root (Spatholobus littoralis Hassk) Water Extract’s Tablet." Journal of Pharmaceutical Sciences and Community 21, no. 1 (2024): 17–22. http://dx.doi.org/10.24071/jpsc.005765.

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Kalimantan's people drink bajakah roots as a traditional medicine to restore stamina and treat various diseases. The infusion is less practical and unstable, so it was developed into a tablet. Porang is a local tuber that contains amylum and amylopectin. The combination of starch-lactose has been widely used as a tablet filler and produces tablets with good physical properties. This study aimed to determine the effect of the combination of porang starch-lactose on the granules and tablets' physical properties. Bajakah roots were infused and dried using a freeze-dryer. The antioxidant activity

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Azizah, Nur, Noval Noval, and Putri Vidiasari Sudarsono. "Optimasi Formulasi Tablet Lepas Lambat Ekstrak Seledri (Apium graveolens L.) Menggunakan Polimer Xanthan Gum dan Lubrikan Magnesium Stearat dengan Metode Simplex Lattice Design (SLD)." Jurnal Surya Medika 9, no. 1 (2023): 180–94. http://dx.doi.org/10.33084/jsm.v9i1.5165.

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Antihypertensive drugs undergo first-pass metabolism and therefore have low oral bioavailability. It causes an increase in the frequency of drug use and concentration fluctuations that affect patient comfort. The sustained release tablet formulation was chosen because it can deliver the active substance with good bioavailability. An active antihypertensive substance that can be used is celery extract because it contains flavonoids, so a sustained release tablet formulation was made using xanthan gum and magnesium stearate to produce a constant and controlled release rate. This study aims to kn

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Shubham Tiwari, Satish Kumar Sarankar, Sushma Somkuwar, and Sushma Somkuwar. "Formulation and evaluation of ranitidine floating tablet." International Journal of Frontiers in Biology and Pharmacy Research 3, no. 1 (2022): 046–52. http://dx.doi.org/10.53294/ijfbpr.2022.3.1.0022.

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The aim of present investigation is to formulate floating tablet to increase duration of action of ranitidine. Floating tablet of ranitidine has long duration of action as compare to its sustained release formulation, Floating tablet has double duration of action than sustained release formulation. Floating tablet is developed by using various polymers like HPMC (15000) and few grades of carbopol, citric acid and sodium bicarbonate were added for effervescence. Tablets were prepared by wet granulation technique by using single operation punch machine in different formulation with polymers, als

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Y., Shiva Kumar* Dr.T. Mangilal Dr. M. Ravi Kumar J. Naveen. "PREPARATION AND EVALUATION OF TAPENTADOL MOUTH DISSOLVING TABLETS." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES o6, no. 04 (2019): 8726–36. https://doi.org/10.5281/zenodo.2656643.

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<em>Mouth dissolving tablets are solid dosage forms containing tapentadol as active pharmaceutical ingredient which has analgesic effect, and has superdistegrants like croscarmellose sodium and starch glycolate which disintegrates fast usually less than 60 seconds without the need of water when placed on the tongue. To prepare and evaluate tapentadol mouth dissolving tablet by using direct compression method  and to determine the effect of formulation process and the excipients. Tapentadol MDT were formulated by using ingredients and superdisintegrants like sodium starch glycolate and cro

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Mehetre, Gautam D., Rameshwar S. Cheke, and Vinayak N. Shrikhande. "Formulation and In-Vitro Evaluation of Enteric Coated Tablet Incorporating Rabeprazole." Journal of Drug Delivery and Therapeutics 10, no. 2-s (2020): 50–57. http://dx.doi.org/10.22270/jddt.v10i2-s.3953.

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The objective of the work is to try and assess the applicability and manufacturing possibilities to optimize an enteric coated tablet formulation containing Rabeprazole sodium as the drug aiming at the anti-acidity activity with desired drug release properties. Enteric coated tablet was chosen as dosage form being a cost-effective technology for pharmaceutical industry requiring fewer procedures. Before the implementation of the pharmaceutical technological aims, analysis of critical factors influencing the manufacture was carried out. Reproducible manufacturing processes are required to achie

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Manish, Kumar Gupta, Ghadge Madhvi, Verma Sunil, and Singh Sudharshana. "FORMULATION AND EVALUATION OF BILAYER TABLETS FOR SUSTAINED RELEASE." International Journal of Current Pharmaceutical Review and Research 13, no. 3 (2021): 38–43. https://doi.org/10.5281/zenodo.12667170.

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Bi-layer tablet is a new era for successful development of controlled release formulationalong with various features to provide successful drug delivery. Bilayer layer tablets consistof two layers which are slow release and immediate release layers. It is an improvedtechnology to overcome the shortcoming of the single layer tablets and offer more benefits.The bilayer tablet helps to separate incompatible active pharmaceutical ingredient (APIs)from each other. Bilayer tablets material involves both the compressibility and consolidation.Bilayer formulations carry different drugs in each layer an

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Noval, Noval, Rizka Appriliani, and Husda Oktaviannoor. "Evaluasi Pengaruh Konsentrasi Pati Biji Cempedak (Artocarpus champeden) sebagai Bahan Pengisi pada Formulasi Tablet Paracetamol." Jurnal Surya Medika 6, no. 2 (2021): 111–18. http://dx.doi.org/10.33084/jsm.v6i2.2127.

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Cempedak plants are widely distributed in Indonesia, one of which is Kalimantan. Cempedak is a tropical plant, so its potential can be used as an additive in the manufacture of pharmaceutical preparations. Previous studies used cempedak seed starch as a binding agent in tablet formulations. This study aims to determine the effect of variations in concentration and optimum concentration of Cempedak seed starch (Artocarpus champeden) as a filler for Paracetamol tablets. The study used a True Experimental Design design with a posttest-only control group design. Making tablets using the wet granul

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Penabaka VenugopalaiahPenabaka Venugopalaiah, KP Benidicts Prem Prakash, Yerikala Ramesh, and M Alagusundaram. "Formulation and evaluation of extended-release tablets of trimetazidine HCL." World Journal of Advanced Research and Reviews 18, no. 3 (2023): 993–1002. http://dx.doi.org/10.30574/wjarr.2023.18.3.1003.

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The present study was undertaken with an aim to formulate develop and evaluate Trimetazidine HCL extended release matrix tablets using different polymers as release retarding agent. Pre formulation study was done initially and results directed for the further course of formulation. Based on Pre formulation studies different batches of Trimetazidine HCL were prepared using selected excipients. Powders were evaluated for tests Angle of repose, Bulk density, tapped density, compressibility index, and Hausner ratio before being punched as tablets. It was concluded that the tablets of batch F9 had

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Penabaka, Venugopalaiah, Benidicts Prem Prakash KP, Ramesh Yerikala, and Alagusundaram M. "Formulation and evaluation of extended-release tablets of trimetazidine HCL." World Journal of Advanced Research and Reviews 18, no. 3 (2023): 993–1002. https://doi.org/10.5281/zenodo.8434813.

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The present study was undertaken with an aim to formulate develop and evaluate Trimetazidine HCL extended release matrix tablets using different polymers as release retarding agent. Pre formulation study was done initially and results directed for the further course of formulation. Based on Pre formulation studies different batches of Trimetazidine HCL were prepared using selected excipients. Powders were evaluated for tests Angle of repose, Bulk density, tapped density, compressibility index, and Hausner ratio before being punched as tablets. It was concluded that the tablets of batch F9 had

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Kulkarni, Vaishnavi M., Shubham B. Babare, Sanket K. Joshi, et al. "Formulation and Evaluation of Paracetamol Tablets using Coconut Oil as a Binder." Journal of Drug Delivery and Therapeutics 12, no. 1-S (2022): 4–7. http://dx.doi.org/10.22270/jddt.v12i1-s.5320.

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Tablets are the medicament with suitable excipients. It comprises a mixture of active substances and excipients, usually pressed or compacted from a powder into a solid dose. The aim of this study was to formulate paracetamol tablets using Coconut oil as a binder in different concentrations (1%, 2%, 3%) and evaluate them with basic parameters. The granules manufactured using the binder had good flow property and compressibility. There are various examples of binders that can be used for tablet formulation. Here the efforts were made to formulate the paracetamol tablets by using coconut oil to

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Gusfarendi and Wintari Taurina. "AMILUM TEST WASTE OF PALM OIL (Elaeis guineensis Jacq.) AS A BINDER ON PARASETAMOL TABLETS." JURNAL BORNEO AKCAYA 1, no. 1 (2014): 46–54. http://dx.doi.org/10.51266/borneoakcaya.v1i1.9.

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Palm trunk the waste from rejuvenation of the palm plantation. This research was aim to test starch from palm trunk that used as binder in paracetamol tablet. This research used experimental method, which there was three formulas that used starch from palm trunk as a binder with variety concentrations of the F1(5%), F2(10%), F3(15%) and three comparative formulas that used amprotab as a binder with variety concentrations of the F4(5%), F5(10%), F6(15%). Wet granulation method was used to make the tablet. The tablet has evaluated and was statistical analiyzed One Way Anova. Evaluation of the ta

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Ramya, Patnala, Abhaya Diya, Aysha Reslin, et al. "Formulation and Evaluation of Herbal Facewash Tablet." International Journal of Pharmaceutical Research and Applications 10, no. 1 (2025): 1162–67. https://doi.org/10.35629/4494-100111621167.

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The formulation of a herbal facewash tablet incorporating liquorice (Glycyrrhizaglabra) and neem (Azadirachta indica) aims to provide a natural, effective, and convenient skin care solution. Both liquorice and neem are renowned for their therapeutic properties, with antinflammatory and antioxidant benefits, while neem is known for its antimicrobial, antiinflammatory, and purifying effects. In this study, herbal extracts of liquorice and neem we combined to create a tablet-based facewash, which promises gentle yet effective cleansing, while nourishing and protecting the skin. The tablets were d

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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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Maraie, Nidhal K., and Wid F. Neamah. "Preparation and Evaluation of Ophthalmic Ketorolac Tromethamine Minitablet." INTERNATIONAL JOURNAL OF DRUG DELIVERY TECHNOLOGY 13, no. 01 (2023): 193–98. http://dx.doi.org/10.25258/ijddt.13.1.29.

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Objective: The current research is for improving patient compliance by reducing dosing frequency of ocular ketorolac tromethamine used for allergic conjunctivitis through preparation of minitablet for ocular insertion. Method: Ocular mini tablet was prepared by direct compression method using xanthan gum, chitosan and carbopol 943P as polymers to prepare the mini tablet for ocular insertion. The mini tablets were evaluated for drug content, weight variation, bioadhesion, water uptake and swelling behavior, in vitro drug release and ocular irritation. Results: The best formula (F1) containing 1

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Vaishnavi, Raskar* Tanaya Wackchaure. "Formulation And Evaluation of Antitussive Tablet of Ginger." International Journal of Pharmaceutical Sciences 3, no. 6 (2025): 1071–76. https://doi.org/10.5281/zenodo.15605468.

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Zingiber officinal, species of the ginger family Zingiberaceae has a long history of medicinal use for more than 2000 years as one of the most versatile medicinal plants having a wide spectrum of biological activity and a common condiment for various foods and beverages. Currently, there is a renewed interest in ginger, and several scientific investigations aimed at isolation, identification of active constituents , scientific verification of its pharmacological actions for treatment of several diseases and conditions. Solid Dosage Forms are popular as case of administration, accurate dosage,

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Yayehrad, Ashagrachew Tewabe, Tesfa Marew, Motlalepula Matsabisa, and Gebremariam Birhanu Wondie. "Physicochemical Characterization and Evaluation of Ficus vasta Gum as a Binder in Tablet Formulation." BioMed Research International 2023 (August 9, 2023): 1–18. http://dx.doi.org/10.1155/2023/8852784.

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Binders are ingredients used in tablet granulation process for tablet cohesiveness which confirms that the tablet remains intact after compression. Natural gums have been employed as disintegrants, emulsifying agents, suspending agents, and binders in tablets. Even though Ficus vasta gum is claimed as a possible pharmaceutical excipient by some phytochemical studies, literature is scanty on its efficacy as a tablet binder. The purpose of this study was to isolate, characterize, and comparatively evaluate Ficus vasta gum as a potential binder in tablet formulation. Gum was extracted from Ficus

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Patha, S., P. Dara, S. K. Yamsani, R. Thadkapally, and J. Aukunuru. "DEVELOPMENT AND EVALUATION OF ORAL ELEMENTARY OSMOTIC PUMP TABLETS FOR ROPINIROLE HYDROCHLORIDE." INDIAN DRUGS 49, no. 06 (2012): 23–30. http://dx.doi.org/10.53879/id.49.06.p0023.

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The objective of the present study was to develop a sustained release once a day oral elementary osmotic tablet for ropinirole hydrochloride and evaluate its in vivo performance. The core of elementary osmotic tablet of ropinirole hydrochloride was prepared by compression of mixture consisting of drug,different concentrations of osmogens, and other tablet material. Core tablets were then coated with different concentrations of cellulose acetate and PEG-400. FTIR was used to identify if the excipients are compatible with the drug. All the tablets that were prepared were evaluated for drug relea

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Kumar, Damit, Amit Sharma, and Rajiv Garg. "FORMULATION AND EVALUATION OF SUBLINGUAL TABLET OF LOSARTAN POTASSIUM." Asian Journal of Pharmaceutical Research and Development 6, no. 4 (2018): 54–66. http://dx.doi.org/10.22270/ajprd.v6i4.386.

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The objective of the current study was to develop and optimize a sublingual tablet of Losartan potassium, which is an effective drug in the treatment of hypertension. Owing to number of advantages dissociated with the quick onset of action and it by passes the liver. Sublingual tablets offer effective and easier way for management of Hypertension. The basic approach used in development of Sublingual tablet was the use of super disintegrants by direct compression method. Oral mucosal drug delivery is one of the promising method of systemic drug delivery which offers several advantages. The lite

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ABDULLAHI, ABBA KHALID, ADENIJI KEHINDE OLOWOSULU, and TERYILA SUZANNE ALLAGH. "Preparation and Evaluation of Metronidazole Tablets Produced with Different Binders Using Wet Granulation Method." Malaysian Journal of Pharmaceutical Sciences 22, no. 1 (2024): 87–104. http://dx.doi.org/10.21315/mjps2024.22.1.6.

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In tablet formulation, binders are essential for ensuring proper powder mix, granulation and overall tablet quality. Variations in binder quality and concentration can impact drug bioavailability, strength and manufacturing processes. The inconsistency in bioavailability and therapeutic response of metronidazole from different manufacturers highlights the importance of binder selection in tablet formulation. This study evaluates the impact of different binding agents on tablet quality. The optimum binder concentration for each of the binders was assessed to obtain suitable concentration that w

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Alkarib, Suad Y., and Deina E. MohamedElhassan. "Evaluation of Acacia- Guar Gum Combination as Delayed Release Coating Former on Solid Placebo Tablets." Journal of Advanced Pharmaceutical Science And Technology 2, no. 4 (2021): 1–10. http://dx.doi.org/10.14302/issn.2328-0182.japst-21-3700.

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Objectives The present study addresses evaluation of acacia-guar gum combination as an enteric former for tablet coating aiming to add knowledge on how develop the ability of enteric forming ability of acacia-guar combination. Methods Five formulations of enteric coating solution incorporating guar gum as delayed release polymers along with film coating material acacia gum followed by CMC and glycerin as plasticizer and coloring agents were prepared to coat placebo tablet cores. Different enteric coating formulations organized in different acacia : guar gum ratios as 1:1, 1:2, 1:3, 1:4 and 1:6

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Padang, Assaini Carinta, and Haerawati Idris. "Evaluation of Iron Tablet Program Among Pregnant." Media Kesehatan Masyarakat Indonesia 15, no. 4 (2019): 319. http://dx.doi.org/10.30597/mkmi.v15i4.7399.

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Anemia was one of the health problems throughout the world, especially in developing countries. The purpose of this study was to evaluate the program of iron tablets among pregnant women. This study used the CIPP evaluation model approach (Context, Input, Process, and Product). The Informant selected by the purposive method. The technique of data collection was done through in-depth interviews, document review, and observation. Data analysis was done by content analysis. The results of the study showed the components of the context of the birth of the blood supplement tablet program to reduce

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Bohlouli, Sepideh, Safa Raeesi, Hossein Samadi Kafil, Ramin Negahdari, Mohammad Hassani, and Zahra Aghazadeh. "Evaluation of Antifungal Effects of Tablets containing Ginger on Dentures Contaminated with Candida (In Vitro)." Avicenna Journal of Dental Research 15, no. 1 (2023): 5–9. http://dx.doi.org/10.34172/ajdr.2023.457.

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Background: Denture stomatitis (DS) due to Candida albicans is a chronic inflammation of mucous membranes that occurs beneath acrylic resin dentures. Various antifungal and disinfecting agents with different formulations are used to treat this condition with different side effects. Recently, the use of herbal medicines has attracted attention in the treatment of medical and dental conditions. The main goal of this study was to evaluate the antifungal efficacy of effervescent tablets containing ginger on complete dentures in patients with oral fungal infections in vitro. Methods: In the present

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Kittipongpatana, Ornanong S., Karnkamol Trisopon, Phanphen Wattanaarsakit, and Nisit Kittipongpatana. "Utilization and Evaluation of Rice Bran and Rice Bran Wax as a Tablet Lubricant." Pharmaceutics 16, no. 3 (2024): 428. http://dx.doi.org/10.3390/pharmaceutics16030428.

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The rice bran and rice bran wax of the KJ CMU107 rice strain were investigated as potential tablet lubricants in a directly compressed tablet formulation. Stabilized full-fatted rice bran (sFFRB), stabilized defatted rice bran (sDFRB), and rice bran wax (RBW) extracted and purified from crude rice bran oil (cRBO) were tested. Two commercial lubricants, including magnesium stearate (MGS) and hydrogenated cottonseed oil (HVO), were employed as the standards in the formulated mixtures, which contained spray-dried rice starch (SDRS) as a diluent. The tableting was carried out for each formulation,

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N, Audinarayana, Anala Srinivasulu, Vellore Sruthikumari, Likitha, and Ananda Deepak V. "Colon targeting oral matrix tablets of mesalamine: Design, development and invitro evaluation." International Journal of Novel Trends in Pharmaceutical Sciences 10, no. 1 (2020): 18–27. http://dx.doi.org/10.26452/ijntps.v10i1.1144.

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The principle in this present research is to formulate Mesalamine containing colon targeted tablets by using different polymers and evaluate the effect of different polymers in drug release pattern. The matrix tablets of Mesalamine are formulated by polysaccharides based polymers like Cellulose acetate phthalate (CAP), Ethyl cellulose (EC), Guar gum (GG) and Xanthan gum (XG) which protects the drug to release in Stomach and Small Intestine. The invitro drug dissolution investigation of F2 (GG and XG) Matrix tablet was controlled by swelling into a viscous gel in colonic pH, which have been acc

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Ferguson, Jacqueline M., James Van Campen, Cindie Slightam, Liberty Greene, Leonie Heyworth, and Donna M. Zulman. "Evaluation of the Veterans Health Administration’s Digital Divide Consult for Tablet Distribution and Telehealth Adoption: Cohort Study." Journal of Medical Internet Research 26 (September 9, 2024): e59089. http://dx.doi.org/10.2196/59089.

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Background Video telehealth offers a mechanism to help Veterans Health Administration (VHA) patients overcome health care access barriers; however, many veterans lack a suitable device and sufficient internet connectivity. To address disparities in technology access, VHA established a Connected Device Program that offers veterans loaned video-capable tablets and internet service. In 2020, VHA introduced a national Digital Divide Consult to facilitate and standardize referrals for this resource. Objective We sought to evaluate the reach and impact of VHA’s Connected Device Program, leveraging D

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MAHAJAN, NILESH M., Kalyanee Wanaskar, Yogesh Bhutada, Raju Thenge, and Vaibhav Adhao. "DESIGN AND IN VITRO EVALUATION OF EXTENDED RELEASE TABLET OF NATEGLINIDE." Journal of Drug Delivery and Therapeutics 8, no. 5-s (2018): 235–39. http://dx.doi.org/10.22270/jddt.v8i5-s.2012.

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The aim of present study is to formulate and evaluate extended release matrix tablet of Nateglinide by direct compression method using different polymer like HPMC K4 and HPMC K15. Matrix tablet of nateglidine were prepared in combination with the polymer HPMC K4, HPMC K15, along with the excipients and the formulations were evaluated for tablet properties and in vitro drug release studies. Nateglinide matrix tablet prepared by using polymer such as HPMC K4 and HPMC K15, it was found that HPMC K15 having higher viscosity as compare to HPMC K4 therefore different concentration of polymer were st

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