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Journal articles on the topic 'And patient-friendly dosage'

Author: Grafiati

Published: 7 June 2025

Last updated: 16 July 2025

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1

Rameesa, C. K., and M. K. Drisya. "ORODISPERSIBLE TABLET: A Patient Friendly Dosage Form (a Review)." Bali Medical Journal 4, no. 1 (2015): 17. http://dx.doi.org/10.15562/bmj.v4i1.101.

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Bhoyar, P. K., D. M. Biyani, and M. J. Umekar. "Formulation and Characterization of Patient-Friendly Dosage Form of Ondansetron Hydrochloride." Journal of Young Pharmacists 2, no. 3 (2010): 240–46. http://dx.doi.org/10.4103/0975-1483.66796.

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Waghulde, Sandeep, Archana Pawar, Minal Kadav, Pratiksha Khade, and Mohan Kale. "Formulation development of patient friendly dosage form for eye drug delivery: Kajal." Journal of Pharmacognosy and Phytochemistry 7, SP6 (2018): 31–34. http://dx.doi.org/10.22271/phyto.2018.v7.isp6.1.08.

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Waghulde, Sandeep, Archana Pawar, Minal Kadav, et al. "Formulation Development of a Patient Friendly Dosage Form for Eye Drug Delivery: Kajal." Proceedings 9, no. 1 (2018): 69. http://dx.doi.org/10.3390/ecsoc-22-05663.

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Traditionally, kajal is known as kohl or surma and is used as eyeliner. Designing herbal kajal with medicinal plants as a cosmetics product is considered to bea novel, innovative technique. The main advantages of such a product are that it is patient friendly, water resistant, stable, and economical to formulate. Two medicinal plants, viz., Rosa rubiginosa and Triphala, were evaluated for their potential for sustained ocular delivery with the aim of formulating herbal kajal. Standardization of the herbs was performed based on different physiochemical parameters, and the obtained values were wi

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Prajapat, Priyanka, Dilip Agrawal, and Gaurav Bhaduka. "A brief overview of sustained released drug delivery system." Journal of Applied Pharmaceutical Research 10, no. 3 (2022): 05–11. http://dx.doi.org/10.18231/j.joapr.2022.10.3.5.11.

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The most popular and patient-friendly method of drug administration is often thought to be the oral route of administration. Compared to conventional release formulations, advancements in formulation technology, including modified release dosage forms or sustained release oral dosage forms, have been extensively accepted. A sustained release dosage form provides a prolonged release of the drug over an extended period, thereby giving better patient compliance and enhanced bioavailability. Sustain release systems are considered a wiser approach for drugs with short half-lives requiring repeated

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Zanolla, Debora, Serena Bertoni, Nadia Passerini, Beatrice Albertini, Guglielmo Zingone, and Beatrice Perissutti. "From Bitter to Sweet: a preliminary study towards a patient-friendly Praziquantel dosage form." Comptes Rendus. Chimie 25, G1 (2022): 179–88. http://dx.doi.org/10.5802/crchim.188.

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Bernini, Maristella, K. Binuraj, Manish Kumar Gupta, Albertina Arien, and Kaustubh Tambwekar. "Development of age appropriate, patient friendly and flexible dosage forms of an anticancer compound." International Journal of Pharmaceutics 511, no. 2 (2016): 1140–41. http://dx.doi.org/10.1016/j.ijpharm.2016.06.091.

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Golhen, Klervi, Michael Buettcher, Jonas Kost, Jörg Huwyler, and Marc Pfister. "Meeting Challenges of Pediatric Drug Delivery: The Potential of Orally Fast Disintegrating Tablets for Infants and Children." Pharmaceutics 15, no. 4 (2023): 1033. http://dx.doi.org/10.3390/pharmaceutics15041033.

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A majority of therapeutics are not available as suitable dosage forms for administration to pediatric patients. The first part of this review provides an overview of clinical and technological challenges and opportunities in the development of child-friendly dosage forms such as taste masking, tablet size, flexibility of dose administration, excipient safety and acceptability. In this context, developmental pharmacology, rapid onset of action in pediatric emergency situations, regulatory and socioeconomic aspects are also reviewed and illustrated with clinical case studies. The second part of

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Trofimiuk, Monika, Katarzyna Wasilewska, and Katarzyna Winnicka. "How to Modify Drug Release in Paediatric Dosage Forms? Novel Technologies and Modern Approaches with Regard to Children’s Population." International Journal of Molecular Sciences 20, no. 13 (2019): 3200. http://dx.doi.org/10.3390/ijms20133200.

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In the pharmaceutical technology, paediatric population still presents the greatest challenge in terms of developing flexible and appropriate drug dosage forms. As for many medicines, there is a lack of paediatric dosage forms adequate for a child’s age; it is a prevailing practice to use off label formulations. Children need balanced and personalized treatment, patient-friendly preparations, as well as therapy that facilitates dosing and thus eliminates frequent drug administration, which can be ensured by modified release (MR) forms. MR formulations are commonly used in adult therapy, while

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Mohapatra, Ashutosh, RajeshK Parikh, and MukeshC Gohel. "Formulation, development and evaluation of patient friendly dosage forms of metformin, Part-I: Orally disintegrating tablets." Asian Journal of Pharmaceutics 2, no. 3 (2008): 167. http://dx.doi.org/10.4103/0973-8398.43304.

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Mohapatra, Ashutosh, RajeshK Parikh, and MukeshC Gohel. "Formulation, development and evaluation of patient friendly dosage forms of metformin, Part-II: Oral soft gel." Asian Journal of Pharmaceutics 2, no. 3 (2008): 172. http://dx.doi.org/10.4103/0973-8398.43305.

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Mohapatra, Ashutosh, RajeshK Parikh, and MukeshC Gohel. "Formulation, development and evaluation of patient friendly dosage forms of metformin, Part-III: Soluble effervescent tablets." Asian Journal of Pharmaceutics 2, no. 3 (2008): 177. http://dx.doi.org/10.4103/0973-8398.43306.

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Sjöholm, Erica, Rathna Mathiyalagan, Xiaoju Wang, and Niklas Sandler. "Compounding Tailored Veterinary Chewable Tablets Close to the Point-of-Care by Means of 3D Printing." Pharmaceutics 14, no. 7 (2022): 1339. http://dx.doi.org/10.3390/pharmaceutics14071339.

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Certain patient populations receive insufficient medicinal treatment due to a lack of commercially available products. The number of approved veterinary products is limited, making animals a patient population with suboptimal medicinal treatments available. To answer to this unmet need, compounding and off-label use of human-marketed products are practiced. Both of which have a significant risk of preparation errors. Hence, there is a dire demand to find and implement a more automated approach to the accurate, precise, and rapid production of veterinary dosage forms close to the point-of-care.

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Huang, Chen-Yu, Guan-Yeu Chen, Miawh-Lirng Shieh, and Hsin-Yang Li. "Validating the Use of Corifollitropin Alfa in Progestin-Primed Ovarian Stimulation Protocol on Normal and High Responders by Comparing with Conventional Antagonist Protocol: A Retrospective Study." Life 10, no. 6 (2020): 90. http://dx.doi.org/10.3390/life10060090.

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Our previous study showed a satisfactory reproductive outcome resulting from the patient-friendly ovarian stimulation protocol using long-acting follicle stimulation hormone (FSH) plus oral medroxyprogesterone acetate (MPA). The present retrospective study aims to compare the efficacy of the patient-friendly ovarian stimulation protocol with that of the antagonist protocol on normal and high responders aged between 24 and 39 years in a tertiary fertility center in Taiwan. To prevent premature luteinizing hormone (LH) surge, oral MPA was given to patients in group 1 (n = 57), whereas antagonist

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Surendran, Emy S., Sinimol T P, and Sreedeepthi G N. "A REVIEW ON KWATHA EXTRACT SACHETS: A PRESERVATIVE FREE AND PATIENT FRIENDLY ALTERNATIVE DOSAGE FORM OF THE TRADITIONAL KWATHA." International Journal of Research in Ayurveda and Pharmacy 12, no. 2 (2021): 104–6. http://dx.doi.org/10.7897/2277-4343.120256.

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Ayurveda is a science with deep insight and keen observation. It is rich in an exquisite collection of medicinal preparations suitable in diverse conditions. Kwatha kalpana/kwatha (decoction) which is a highly significant and an inevitable form of medication in almost all prescriptions by an Ayurvedic physician is the primary subject of this study. It is a water-based preparation to extract active compounds from medicinal plant materials. The classical textbooks of Ayurveda, insists on the administration of Kwatha immediately after preparation, while it is warm. But it is quite difficult to di

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Ravula, Tulasi Naga Pavan Kumar* Boddani Sunil Pattem Sirsha Suma Sri Potti Ayennedi Kusuma Lalitha Mane Kota Vinay Kumar Panja Aishwarya Sai Nuthipalli Joshna Kukala Lavanya Jyothi. "Formulation and Evaluation of Kalanchoe Pinnata Syrup: A Pharmaceutical Dosage Form for Treatment Urolithiasis (Renal calculus) and UTI." International Journal of Pharmaceutical Sciences 3, no. 2 (2025): 1123–31. https://doi.org/10.5281/zenodo.14872675.

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This research focuses on the formulation and evaluation of a herbal syrup containing Kalanchoe pinnata extract, targeting urolithiasis (renal calculus) management. Kalanchoe pinnata, widely recognized for its anti-inflammatory, nephroprotective, and antimicrobial properties, is a promising therapeutic agent for urinary and renal conditions. The objective was to develop a stable, palatable, and patient-friendly dosage form to enhance compliance, particularly for individuals with urinary tract disorders and kidney stones.   The syrup formulation was prepared using a standardized ethano

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Liew, Kai Bin, Ganesan Gobal, Hanifah Mohd Rofiq, et al. "Orally Disintegrating Film: A Review of Its Formulation and Manufacturing Method." NOVEMBER 2023 19, no. 6 (2023): 297–303. http://dx.doi.org/10.47836/mjmhs.19.6.39.

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Oral route drug delivery system is still considered as the most convenient and patient friendly drug delivery route. Over the decades, many research has been performed to improve the functionality oral dosage form. Orally disintegrating film (ODF) is a newer oral drug delivery system, which is in the form of a thin film that will disintegrate in the oral cavity within a matter of seconds. The aim of this review paper is to recap ODF, its benefits, formulation contents and manufacturing method. With more research and development work has been conducted on ODF, the dosage form is expected to be

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Komal, Khade, Kulkarni Nilesh, Bhamare Vaibhav, and Amrutkar Rakesh. "Formulation, Development and Characterization of Oral Jelly to Improve Therapeutic Effectiveness." INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE 15, no. 02 (2024): 1023–34. http://dx.doi.org/10.25258/ijpqa.15.2.73.

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The oral route is the most convenient and has great effectiveness in taking new chemical entities; hence it has improved patient acceptance. However, the main limitations associated with such formulations involve unpleasant or bitter taste as well as problems related to swallowing and reduced bioavailability of chemical entities. When it comes to children, the main limitation is they cannot safely swallow the medications in the form of tablets and capsules. But kids, even those without teeth, can swallow the jelly easily. As in the development of new dosage forms for every child, taste, color,

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Zaytsev, A. A., and A. I. Sinopalnikov. "The problem of patient compliance with treatment for respiratory infections." Medical Council, no. 15 (December 8, 2019): 63–69. http://dx.doi.org/10.21518/2079-701x-2019-15-63-69.

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Patient compliance describes the degree, to which a patient follows treatment regimen. At present, non-compliance with medical recommendations is one of the key problems for outpatient practice. Even in case of respiratory infections, patients often violate the prescribed treatment regimen, which leads to growth of ineffective treatment cases, complications, and is also accompanied by a high risk of selection of drug-resistant infectious organisms and rise in expenditures for managing patients. The most common mistakes made by patients include the change by patients of the prescribed antibioti

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20

Białek, Antoni, Julia Krysztofiak, Aleksandra Hozakowska, et al. "Novel Soft Dosage Forms for Paediatric Applications: Can We 3D-Print Them or Not?" Gels 11, no. 3 (2025): 187. https://doi.org/10.3390/gels11030187.

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Over the past years, numerous novel dosage forms, including gels, have been investigated for paediatric treatment due to the need to provide flexible dose adjustment possibilities, as well as a patient-friendly approach to drug delivery. Simultaneously, 3D printing technology is continuously advancing and gaining interest as a tool for personalised formulation development. Multiple additive manufacturing methods, including the semi-solid extrusion, especially used in gel printing, provide flexibility regarding the dose of active ingredients and the adjustment of the design of soft dosage forms

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SA, Vadivel, Sibichanduru E, Saravanan S, and Karthik S. "Formulation and Evaluation of Cefixime Pediatric Medicated Lollipops." INTERNATIONAL JOURNAL OF DRUG DELIVERY TECHNOLOGY 14, no. 04 (2024): 1071–76. https://doi.org/10.25258/ijddt.14.4.22.

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The study explores the formulation and evaluation of Cefixime medicated lollipops as a novel solution for paediatric oral drug delivery. The developed lollipops demonstrated desirable physical and pharmaceutical attributes, including consistent drug content, optimal hardness, and adherence to weight variation standards. Fourier-transform infrared spectroscopy confirmed the absence of significant drug-excipient interactions, ensuring formulation stability. Among the tested formulations, F2 exhibited the most promising results, achieving 100.05% cumulative drug release within 15 minutes during I

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Das, Sahil1* Painuly Neelam2. "Formulation And Evaluation Of Herbal Effervescent Tablets For The Treatment Of Constipation." International Journal in Pharmaceutical Sciences 2, no. 6 (2024): 736–45. https://doi.org/10.5281/zenodo.11622689.

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The formulation and evaluation of herbal effervescent tablets for constipation were conducted to develop a natural, effective, and patient-friendly treatment option. Four formulations were prepared using Indian Senna, Psyllium husk, Bael fruit pulp, and other excipients. The tablets were assessed for weight variation, hardness, friability, effervescence time, and disintegration time. All formulations met the weight variation limit, indicating uniformity in dosage. Tablet hardness ranged from 5.8 to 8.3 N, ensuring appropriate mechanical strength. Friability values were below 1%, signifying tab

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Das, Sahil1* Painuly Neelam2. "Formulation And Evaluation Of Herbal Effervescent Tablets For The Treatment Of Constipation." International Journal in Pharmaceutical Sciences 2, no. 6 (2024): 736–47. https://doi.org/10.5281/zenodo.11666060.

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The formulation and evaluation of herbal effervescent tablets for constipation were conducted to develop a natural, effective, and patient-friendly treatment option. Four formulations were prepared using Indian Senna, Psyllium husk, Bael fruit pulp, and other excipients. The tablets were assessed for weight variation, hardness, friability, effervescence time, and disintegration time. All formulations met the weight variation limit, indicating uniformity in dosage. Tablet hardness ranged from 5.8 to 8.3 N, ensuring appropriate mechanical strength. Friability values were below 1%, signifying tab

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Mandal, Raj Kumar, Paarth Saini, Rahul Pal, Prachi Pandey, and Anshita Dubey. "Coating Tablets, Compositions, Recent Advancement and Current Status: A Comprehensive Review." Journal of Drug Delivery and Therapeutics 14, no. 10 (2024): 182–95. http://dx.doi.org/10.22270/jddt.v14i10.6809.

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Conventional Tablets are solid oral dosage forms that contain an active pharmaceutical ingredient (API) along with excipients. These tablets are typically prepared through direct compression, wet granulation, or dry granulation. They are designed to disintegrate and release the API in a controlled or immediate manner, depending on the formulation. Tablet coating is a vital process in pharmaceutical technology, designed to improve the therapeutic efficacy, patient compliance, and stability of oral dosage forms. This comprehensive review explores the key aspects of tablet coating, including the

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Freter, Susan, and Susan K. Bowles. "Comparison of a Frail-Friendly Nomogram with Physician-Adjusted Warfarin Dosage for Prophylaxis after Orthopaedic Surgery on a Geriatric Rehabilitation Unit." Canadian Journal on Aging / La Revue canadienne du vieillissement 24, no. 4 (2005): 443–47. http://dx.doi.org/10.1353/cja.2006.0007.

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ABSTRACTWarfarin dosing for thromboprophylaxis in post-operative patients is time-consuming. Warfarin-dosing nomograms can be used in post-operative arthroplasty patients, but warfarin requirements are lower in frail older people. We modified an existing post-arthroplasty nomogram to a frail-friendly version and evaluated its performance in a frail elderly post-orthopaedic surgery on a geriatric rehabilitation ward to determine if it would improve quality indicators for oral anticoagulation. On a geriatric rehabilitation unit, post-operative orthopaedic patients were assigned to either physici

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Yadav, Niraj Kumar, Nilesh Gupta, and Umesh Kumar Jain. "Formulation and evaluation of sustained release floating tablets of venlafaxine using natural polymers." Journal of Drug Delivery and Therapeutics 14, no. 6 (2024): 125–30. http://dx.doi.org/10.22270/jddt.v14i6.6611.

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Over the past three decades, oral controlled-release dosage forms have been developed due to their therapeutic advantages, such as ease of administration, patient compliance, and flexibility in formulation. However, this approach has faced physiological difficulties, such as the inability to contain and position the controlled drug delivery system within the desired region of the gastrointestinal tract (GIT) due to variable gastric emptying and motility. Venlafaxine is an antidepressant and a serotonin and norepinephrine reuptake inhibitor (SNRI). Its active metabolite, desvenlafaxine, works b

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P. Samba Siva Rao, P. Samba Siva Rao, Dr G. Nagaraju Dr. G. Nagaraju, A. Sanjay A. Sanjay, et al. "Review on Formulation and Evaluation of Voglibose Mouth Dissolving Tablets." International Journal of Pharmaceutical Research and Applications 10, no. 2 (2025): 309–17. https://doi.org/10.35629/4494-1002309317.

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Mouth dissolving tablets are solid dosage forms which break down in the oral cavity less than one minute without using of water. These dosage forms are placed in the mouth, allowable to diffuse or melt in the saliva. The purpose of this article is to review potential advancements of Oral Dispersible Tablet technology in drug delivery applications. Mouth dissolving Voglibose tablets offer a convenient and patient-friendly alternative to traditional tablets for the management of type 2 diabetes mellitus. With their rapid disintegration and absorption, these tablets provide a quick and effective

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Sahu, Dr Gyanesh Kumar. "Herbal Oral Medicated Jellies: A Novel Approach in Phytopharmaceuticals." INTERANTIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENT 08, no. 12 (2024): 1–7. https://doi.org/10.55041/ijsrem39585.

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Herbal oral medicated jellies represent a novel and patient-friendly approach to phytopharmaceuticals, offering a palatable alternative for delivering therapeutic herbal actives. These dosage forms combine the benefits of natural ingredients with ease of administration, making them particularly suitable for pediatric, geriatric, and other patient populations. This review explores the formulation aspects, including the use of natural polymers, gelling agents, and sweeteners, and discusses their potential applications in managing various conditions such as respiratory ailments, stress, and infla

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Hua, Xueliang, Chen Li, Jason M. Pogue, et al. "ColistinDose, a Mobile App for Determining Intravenous Dosage Regimens of Colistimethate in Critically Ill Adult Patients: Clinician-Centered Design and Development Study." JMIR mHealth and uHealth 8, no. 12 (2020): e20525. http://dx.doi.org/10.2196/20525.

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Background Determining a suitable dose of intravenous colistimethate is challenging because of complicated pharmacokinetics, confusing terminology, and the potential for renal toxicity. Only recently have reliable pharmacokinetic/pharmacodynamic data and dosing recommendations for intravenous colistimethate become available. Objective The aim of this work was to develop a clinician-friendly, easy-to-use mobile app incorporating up-to-date dosing recommendations for intravenous colistimethate in critically ill adult patients. Methods Swift programming language and common libraries were used for

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Bhavesh, Machhi* Aathira Chandran Divyanka Bodas Chandrakant Wadile Pankaj Mandpe. "Recent Advancement: 3D-Printed Orodispersible Film as Pharmaceutical Dosage Forms for Paediatric Patients." International Journal of Pharmaceutical Sciences 3, no. 1 (2025): 1324–38. https://doi.org/10.5281/zenodo.14673092.

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Traditional drug delivery systems are often unsuitable for paediatric patients due to their unique developmental stages and specific dosing requirements are distinct from those of other groups within the population. Oral delivery is recognized as the most user-friendly and popular method in therapeutic practices due to its safety, high patient compliance, ease of administration, affordable price, and flexibility. The challenge of medication adherence is increasingly recognized as a critical public health issue, with poor adherence to treatment linked to negative health consequences and higher

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Sizova, Zh M. "Pharmacotherapeutic approaches targeting stable angina: simple solutions to complex problems." Meditsinskiy sovet = Medical Council, no. 4 (April 20, 2021): 34–40. http://dx.doi.org/10.21518/2079-701x-2021-4-34-40.

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Cardiovascular diseases, especially coronary heart disease (CHD), are the leading cause of disability; various registry data show that the annual mortality rate of such patients is 2–3%. This explains the interest of practitioners in the pharmacotherapy of stable forms of coronary artery disease using current progress in the understanding of the pathogenesis of this disease and treatment compliance. Features of the pathogenesis of CHD in the form of increased myocardial oxygen demand, increased pre- and afterload on the performance of the heart necessitate the prescription of rhythm-reducing d

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Dahanayake, Jeevani Maheshika, Pathirage Kamal Perera, Priyadarshani Galappatty, Hettiarachchige Dona Sachindra Melshandi Perera, and Liyanage Dona Ashanthi Menuka Arawwawala. "Comparative Phytochemical Analysis and Antioxidant Activities of Tamalakyadi Decoction with Its Modified Dosage Forms." Evidence-Based Complementary and Alternative Medicine 2019 (May 2, 2019): 1–9. http://dx.doi.org/10.1155/2019/6037137.

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Background and Objective. Tamalakyadi decoction (TD) is a classical formulation mentioned in authentic traditional medicine text Sarasankshepaya under nasal diseases and used as a remedy for allergic rhinitis. It consists of 12 plant ingredients. Decoction preparations are widely used in Sri Lankan traditional system and considered effective and safe for treating many disorders. However, decoctions have to be used only in fresh state due to shorter shelf life and loss of stability. This decoction preparation method leads to decreasing the patient compliance and is also time consuming. Hence, t

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Suthar, V., M. Gokel, S. Butani, and A. Solanki. "SELF-EMULSIFYING DRUG DELIVERY SYSTEM CONTAINING ACECLOFENAC: DESIGN & DEVELOPMENT USING QUALITY BY DESIGN (QBD) CONCEPT." INDIAN DRUGS 51, no. 06 (2014): 16–26. http://dx.doi.org/10.53879/id.51.06.p0016.

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The aim of the present study was to develop self-emulsifying drug delivery system (SEDDS) of aceclofenac for potential improvement in the in vitro dissolution. The Food and Drug Control Agency (FDCA) has put more stress on the quality, safety and efficacy of the dosage form. The use of design of experiments and quality by Design (QbD) in the development of self emulsifying drug delivery system (SEDDS) containing aceclofenac is demonstrated. The optimum formulation contained Labrafil M 1944 CS, Tween 80 and Transcutol P. The systematic approach enabled us in identifying the design space. The re

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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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Butar-Butar, Maria, Asep Roni, Muhamad Pahlevi, Diki Zaelani, Novaliana Sagita, and Reza Pratama. "Recent Advances in Herbal Effervescent Formulations: Challenges and Opportunities." Sciences of Pharmacy 4, no. 1 (2025): 40–50. https://doi.org/10.58920/sciphar0401311.

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The growing demand for convenient and palatable delivery systems for herbal medicines has significantly increased the interest in herbal effervescent formulations as an alternative to conventional dosage forms. Effervescent dosage forms offer rapid dissolution and the potential for enhanced absorption while masking unpleasant tastes often associated with herbal extracts. However, the successful formulation of herbal effervescent tablets presents unique challenges, including managing the complex physicochemical properties of herbal extracts, ensuring their stability and antioxidant activity wit

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Rehan, Beniwale* Dr. Amol Harsulkar Aniket Kadam Akshay Jadhav Bhumika Bidwaik. "A Comprehensive Review on Medicated Chewing Gum (MCG): A Novel Drug Delivery System." International Journal of Pharmaceutical Sciences 3, no. 3 (2025): 1359–72. https://doi.org/10.5281/zenodo.15030091.

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Medicated chewing gum (MCG) has emerged as an innovative and patient-friendly drug delivery system, offering both local and systemic therapeutic effects. It provides a convenient, non-invasive, and water-free method of drug administration, making it highly suitable for individuals with swallowing difficulties and that requiring on-the-go medication. MCG formulations have been developed for a wide range of therapeutic applications, including dental care, pain management, smoking cessation, and weight control. The ability of MCGs to enhance drug bioavailability through buccal absorption while av

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Qureshi, Tammana Yunus, Aayesha Abbasi, Komal Padme, and Kavita Sawkare. "NOVEL APPROACH TO PEDIATRIC ANTI-NAUSEA: FORMULATING & EVALUATING ONDANSETRON-INFUSED CHOCOLATE." International Journal of Pharmaceutical Sciences and Medicine 9, no. 9 (2024): 29–42. http://dx.doi.org/10.47760/ijpsm.2024.v09i09.002.

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Ondansetron is a widely used anti-emetic for managing nausea and vomiting caused by chemotherapy, gastroenteritis, motion sickness, and morning sickness. Traditional formulations include dispersible tablets, syrups, and injections, but these can be challenging for pediatric patients due to the bitter taste of ondansetron. To enhance palatability and patient compliance, we propose the development of a novel dosage form: ondansetron-infused chocolate. This innovative approach leverages chocolate’s natural appeal to pediatric patients, effectively masking the drug’s bitterness. By utilizing a cho

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MD, Abuzar* Nivedita Chatterjee. "Formulation And Evaluation of Effervescent Tablet." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 3576–87. https://doi.org/10.5281/zenodo.15479544.

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Effervescent tablets represent new solid oral dosage forms characterized by the fast disintegration after contact with water, releasing carbon dioxide and giving a solution or dispersion that can be administered orally. Effervescent tablets are many times more beneficial than other dosage forms such as faster drug absorption, greater patient compliance, better taste masking, and effectiveness in patients who have difficulty in swallowing. The preparation of effervescent tablets involves a delicate proportioning of active pharmaceutical ingredients (APIs) and effervescent materials like citric

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Ashwini, Warnkar* Dr. M. A. Channawar Dr. A. V. Chandewar Anjali Bhansali Anisha Kohale Gaurav Magar. "Design, Development and In-Vitro Characterization of Rapidly Disintegrating Oral Solid Dosage Form." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 4731–49. https://doi.org/10.5281/zenodo.15545054.

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The objective of the present study was to design, develop, and evaluate rapidly disintegrating oral films (RDOFs) of Ketorolac Tromethamine for effective pain management, especially in patients with swallowing difficulties. Oral films offer a convenient and patient-friendly alternative to traditional solid dosage forms due to their rapid disintegration and absorption through the oral mucosa. Ketorolac Tromethamine, a potent non-steroidal anti-inflammatory drug (NSAID), was selected as the active pharmaceutical ingredient due to its rapid onset of action. Various film-forming polymers such as H

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Deore, Prashant, and Jayesh Dwivedi. "Formulation and Development of Solifenacin Succinate Oral Suspension." International Journal of Drug Delivery Technology 15, no. 02 (2025): 01–07. https://doi.org/10.25258/ijddt.15.2.25.

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Solifenacin succinate is prescribed for patients with overactive bladder (OAB) syndrome to address symptoms such as urge incontinence, increased urinary frequency, and urgency. Tablet formulations can be challenging or impossible to administer to patients who are unable or unwilling to swallow solid dosage forms like tablets or capsules. For these patients, a liquid formulation of Solifenacin succinate is a more suitable alternative. The goal was to develop a liquid formulation with reduced astringency and bitterness compared to Solifenacin succinate in its raw form, while ensuring good drug c

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Zakowiecki, Daniel, Peter Edinger, Markos Papaioannou, et al. "Development and Evaluation of Lactose-Free Single-Unit and Multiple-Unit Preparations of a BCS Class II Drug, Rivaroxaban." Pharmaceutics 16, no. 11 (2024): 1485. http://dx.doi.org/10.3390/pharmaceutics16111485.

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Background/Objectives: The aim of the present study was to develop lactose-free formulations of rivaroxaban, a novel oral anticoagulant used for the treatment and prevention of blood clotting. As a BCS Class II drug, rivaroxaban is characterized by poor solubility in aqueous media, posing a significant formulation challenge. Methods: To address this, phosphate-based excipients were employed to prepare both traditional single-unit dosage forms (tablets) and modern multiple-unit pellet systems (MUPS). These formulations were successfully developed and thoroughly evaluated for their physical prop

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Samira Bano, Sanket Kumar, Peeyush Sharma, and Mohamad Taleuzzaman. "Fast-Melt Tablets (FMTs): Revolutionizing rapid relief-an in-depth review of swift dissolve technology." International Journal of Biological and Pharmaceutical Sciences Archive 6, no. 2 (2023): 008–36. http://dx.doi.org/10.53771/ijbpsa.2023.6.2.0087.

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Fast Melt tablets (FMTs) have become a promising alternative to solve a number of issues related to conventional oral dose forms. These tablets are made to quickly dissolve in the mouth and disintegrate, making them a practical and patient-friendly alternative for people who have trouble swallowing conventional solid dosage forms. This review study thoroughly examines the various uses of fast-melt tablets in the pharmaceutical business, as well as formulation strategies, production processes, and manufacturing methods. These tablets have been produced using a variety of methods, each with thei

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Siddiqha, Mrs Ayeesha. "IOT Based Pill Reminder and Monitoring System." International Journal for Research in Applied Science and Engineering Technology 12, no. 4 (2024): 1278–81. http://dx.doi.org/10.22214/ijraset.2024.59988.

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Abstract: Introducing an innovative IoT-based pill reminder and monitoring system, this solution aims to tackle medication nonadherence challenges effectively. Leveraging interconnected devices and advanced sensors, personalized medication reminders are delivered to users, enhancing adherence rates efficiently. Accessible via smartphones or other devices, a user-friendly interface allows patients to configure medication schedules and receive timely reminders tailored to their needs. The system tracks pill intakefor dosage accuracy and provides real-time data to healthcare providers for remote

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Tanuja, Pokharkar*1 Vishal Madankar2. "Nicardipine Hydrochloride Granules Used for Antihypertensive Activity." International Journal of Scientific Research and Technology 2, no. 5 (2025): 486–94. https://doi.org/10.5281/zenodo.15475886.

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Nicardipine hydrochloride, a calcium channel blocker, has demonstrated marked effectiveness in the management of hypertension by inducing vasodilation through relaxation of vascular smooth muscle. This study explores the antihypertensive potential of Nicardipine hydrochloride formulated as controlled-release granules—a novel alternative to conventional oral dosage forms. The granules are engineered to deliver a sustained therapeutic effect, aiming to improve bioavailability, prolong drug action, and enhance patient adherence. Formulation development involved careful selection of excipien

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Di Prima, Giulia, Giuseppina Campisi, and Viviana De Caro. "Amorphous Ropinirole-Loaded Mucoadhesive Buccal Film: A Potential Patient-Friendly Tool to Improve Drug Pharmacokinetic Profile and Effectiveness." Journal of Personalized Medicine 10, no. 4 (2020): 242. http://dx.doi.org/10.3390/jpm10040242.

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Nowadays the therapeutic strategies to manage Parkinson’s Disease are merely symptomatic and consist of administering L-DOPA and/or dopamine receptor agonists. Among these, Ropinirole (ROP) is a widely orally-administered molecule, although it is extensively susceptible to hepatic metabolism. Since literature reports the buccal mucosa as a potentially useful route to ROP administration, the development of novel, effective, and comfortable oromucosal formulations should prove desirable in order to both enhance the therapeutic efficacy of the drug and allow a personalized therapeutic strategy ab

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Trupti, Bhalekar* Kalpana Sable Jaya Mehetre Kiran Dhamak. "Dry Powder Inhalers: A Critical Evaluation Of Their Effectiveness And Accessibility." Int. J. in Pharm. Sci. 1, no. 7 (2023): 288–301. https://doi.org/10.5281/zenodo.8173889.

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A Dry Powder Inhaler (DPI) is a device that inhales dry powdered medicine into the lungs. DPIs are frequently used to treat respiratory conditions like COPD, bronchitis, and asthma. In recent years, interest in DPI as an effective and ecologically friendly method of medication delivery to the lung has increased. Only an effective metering mechanism, a well-chosen device, and an appropriate powder composition will allow a dry powder inhaler to achieve these objectives. The three primary categories are nebulizer, pMDI, and DPI. DPIs, which provide medicine to the lungs in the form of a dry powde

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Ingale, Kalyani. "MED-TRACK." INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENT 09, no. 04 (2025): 1–9. https://doi.org/10.55041/ijsrem46472.

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Abstract The healthcare industry is increasingly leveraging technology to improve patient outcomes and enhance the management of medical routines. This project proposes a comprehensive system designed to assist patients in managing their medication schedules effectively. The Prescription Reader, Reminder, and Nearest Medical Shop Locator with Caretaker Reminder is a multifaceted application that integrates Optical Character Recognition (OCR) technology to scan and digitize handwritten or printed medical prescriptions. Once the prescription is digitized, the system automatically schedules remin

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Vedyashkina, N. V., L. Ignatova, Ye Brazhnikova, Т. Stupnikova, and Zh Shakhmetova. "MICROBIAL EXOPOLYSACCHARIDE-BASED HYDROGELS FOR BURN WOUND HEALING." Experimental Biology 102, no. 1 (2025): 166–77. https://doi.org/10.26577/bb2025102114.

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This review examines innovative approaches to the treatment of burn injuries through the use of microbial polysaccharides, highlighting their unique properties such as wound infection prevention, moisture retention, and acceleration of tissue regeneration. The development of novel, natural-based pharmaceutical formulations in a patient-friendly dosage form is necessitated by the complexity and high cost of burn treatment, which, in severe cases, may result in fatal outcomes. An analysis of the pharmaceutical market in Kazakhstan reveals a shortage of multifunctional anti-burn drugs and a limit

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Mayuri, Pachpol* Dr. Shivshankar Mhaske Tushar Kumbhare Komal Takalkar Sakshi Tathe Shital Susar Kalyani Wankhede Santosh Waghmare. "Herbal Pediatric Edible Jelly for Cough." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 3639–51. https://doi.org/10.5281/zenodo.15481821.

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The increasing demand for natural, safe, and child-friendly pharmaceutical alternatives has led to the exploration of innovative drug delivery systems. This review highlights the formulation, development, and evaluation of a herbal pediatric edible jelly for effective cough management. Designed to enhance palatability and patient compliance, the jelly incorporates well-established herbal ingredients—Tulsi, Vasaka, Licorice, Ginger, and Honey—known for their antitussive, expectorant, demulcent, and soothing properties. To ensure a stable and appealing formulation, pectin and gelatin

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Priyanka Raj G, Bhavya G, Harsha Vardhana M G, and Jashwanth Gowda H U. "A Review of Formulation Techniques and Evaluation Parameters of Fast Dissolving Tablets." Journal of Pharma Insights and Research 2, no. 4 (2024): 212–17. http://dx.doi.org/10.69613/vx91cb41.

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Fast dissolving tablets (FDTs) have gained significant popularity as a convenient and patient-friendly dosage form, particularly beneficial for pediatric, geriatric, and patients with swallowing difficulties. These tablets are formulated to disintegrate or dissolve rapidly in the oral cavity, eliminating the need for water and enhancing patient compliance. This review article provides a comprehensive overview of FDTs, covering various aspects such as their definition, ideal characteristics, advantages, and formulation techniques. The manufacturing methods employed in the development of FDTs ar

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