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Journal articles on the topic 'Natural Dosage Form'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Murata, Yoshifumi, Kyoko Kofuji, Norihisa Nishida, and Ryosei Kamaguchi. "Preparation and Characteristics of Film Dosage Form Natural Polysaccharides." Pharmacology & Pharmacy 02, no. 03 (2011): 194–98. http://dx.doi.org/10.4236/pp.2011.23028.

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2

DEVI, GAYATRI, MALKIET KAUR, MANJU NAGPAL, et al. "Advanced Dosage Form Design: Role of Modified Natural Gums." Asian Journal of Chemistry 33, no. 1 (2020): 1–9. http://dx.doi.org/10.14233/ajchem.2021.22937.

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Gums are naturally occurring segments in plants, which are cheap and abundant. Natural gums and their derivatives are widely used in a pharmaceutical dosage form. These natural materials possess several advantages over synthetic ones being chemically inert, non-toxic, low cost and biodegradable. However, quick degradation in the body, poor mechanical properties and low solubility are few disadvantages. To overcome these disadvantages, natural gums are modified by applying different chemical modification procedures. The modification of gums is done via various methods such as changing functiona

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3

Aruna, V., GV Amruthavalli, and R. Gayathri. "Safety profile of synthetic versus natural Psoralen." Journal of Medical Research 5, no. 5 (2019): 194–97. http://dx.doi.org/10.31254/jmr.2019.5507.

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Psoralen is used widely in the treatment of various skin diseases such as Psoriasis, Vitiligo etc. The Psoralen used for the above purpose is in oral dosage form and the topical dosage form is likely to reduce the severe side effects of oral Psoralen. However the phototoxic effect of Psoralen in topical form limit the medical fraternity from accepting it when compared to oral Psoralen. The safety profile of synthetic Psoralen versus natural Psoralen was done and natural Psoralen was found to be non-genotoxic and exerted least toxicity to keratinocytes and melanocytes when the cells were expose

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

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

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Kirteebala, Pawar, Rajendra Shinde Dhawal, Dhondu Shivgan Dipak, et al. "Natural polymers in pharmaceutical drug delivery: A review." World Journal of Biology Pharmacy and Health Sciences 4, no. 3 (2020): 082–90. https://doi.org/10.5281/zenodo.4430990.

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In pharmaceutical formulation two main ingredients are required which is API and excipient. And excipient contains many components which plays vital role in manufacturing of dosage form as well as improve pharmaceutical parameters of the dosage form. Polymers used in any dosage form as excipient. Polymers have influencing capacity towards drug release and should be compatible, stable, non-toxic and economic etc. Generally, polymers are classified into three categories i.e natural, semi-synthetic and synthetic polymers. Nowadays, many pharmaceutical companies inclined towards using natural poly

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Tirunagari, Mamatha, Nagadivya Nerella, Anupama Koneru, Madihah, Syed Sarfaraz, and M. A. Mushtaq. "Formulation and Evaluation of Pediatric Paracetamol Elixir Using Natural Colorant." International Journal of PharmTech Research 13, no. 3 (2020): 180–85. http://dx.doi.org/10.20902/ijptr.2019.130307.

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Oral dosage forms are most popular among other dosage forms. In terms of bioavailability liquid dosage form is better than that of solid dosage form. In the present scenario monophagic liquid dosage forms such as syrups, elixirs, throat paints, mouth washes, gargles have gained huge popularity. These are very basic preparations which involve brief processes, machineries and are cost effective also. They come in wide range colours and flavors so as to attract the pediatric age group. Currently colors derived from natural sources are given priority compared to synthetic ones. In this study we fo

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Kirteebala Pawar, Dhawal Rajendra Shinde, Dipak Dhondu Shivgan, et al. "Natural polymers in pharmaceutical drug delivery: A review." World Journal of Biology Pharmacy and Health Sciences 4, no. 3 (2020): 082–90. http://dx.doi.org/10.30574/wjbphs.2020.4.3.0101.

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In pharmaceutical formulation two main ingredients are required which is API and excipient. And excipient contains many components which plays vital role in manufacturing of dosage form as well as improve pharmaceutical parameters of the dosage form. Polymers used in any dosage form as excipient. Polymers have influencing capacity towards drug release and should be compatible, stable, non-toxic and economic etc. Generally, polymers are classified into three categories i.e natural, semi-synthetic and synthetic polymers. Nowadays, many pharmaceutical companies inclined towards using natural poly

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8

Santosh Kumar, Rada, and S. Chandana. "Isolation and Characterization of Tamarind Kernel Gum: A Novel Natural Floating Polymer." Journal of Drug Delivery and Therapeutics 9, no. 3 (2019): 473–78. http://dx.doi.org/10.22270/jddt.v9i3.2911.

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Floating drug delivery systems (FDDS) are aimed to retain the drug in the stomach and are useful for drugs that are poorly soluble or unstable in intestinal fluids. The underlying principle is very simple i.e., to make the dosage form less dense than the gastric fluids so that it can float on them. The drug usually keeps floating in the gastric fluid and slowly dissolves at a pre-determined rate to release the drug from the dosage form and maintain constant drug levels in the blood. Several approaches are currently used to retain the dosage form in the stomach. The principle of the floating ta

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9

Yang, Zhijun, and Aiping Lyu. "Rational Design of Dosage form of Medicinal Plant and Natural Product." Planta Medica 89, no. 14 (2023): 1347. https://doi.org/10.1055/s-0043-1774026.

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10

V.I., Opryshko, Мamchur V.I., Nosivets D.S., Prokhach A.V., and Kurt-Ametova A.S. "Effective, safe and rational pharmacotherapy of endogenic progesterone deficiency." Reproductive health of woman 1 (February 26, 2021): 21–25. https://doi.org/10.30841/2708-8731.1.2021.229705.

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Today, the most frequent complication of pharmacotherapy is an allergic reaction, the so-called drug or drug allergy. An allergic reaction can be caused both by the active ingredients and by the excipients included in the composition of the drug to provide a certain dosage form and its physicochemical properties. Vaginal progesterone preparations are characterized by a large variety of dosage forms: gels, tablets and gelatin capsules for intravaginal administration. It is known that the safety and efficacy of pharmacotherapy depend on the active substance, the dosage form, and the base of the

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Roman, Vaishnavi* Gaikwad Rutuja. "Development And Characterization of Lornoxicam Tablets Incorporating Banana Starch as A Superdisintegrating for Enhanced Dissolution." International Journal of Pharmaceutical Sciences 3, no. 4 (2025): 2058–63. https://doi.org/10.5281/zenodo.15232534.

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Orally disintegrating tablets (ODTs) are an emerging trend in novel drug delivery system and have received ever-increasing demand during the last few decades. ODTs are solid unit dosage forms, which disintegrate or dissolve rapidly in the mouth without chewing and water. This type of property in dosage form can be attained by addition of different excipients, in which disintegrants are the key adjuvant. In recent years, several newer agents have been developed known as super-disintegrants. Super-disintegrants are used to improve the efficacy of solid dosage form and influence the release rate

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Muse, Menra, J. S. Dua, and D. N. Prasad. "A REVIEW ON BUCCAL FILM: AN INOVATIVE DOSAGE FORM." INDIAN DRUGS 54, no. 01 (2017): 5–14. http://dx.doi.org/10.53879/id.54.01.10706.

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Buccal administration of drugs leads to systemic circulation through internal jugular vein, bypassing them from hepatic first pass metabolism and leading to greater bioavailability. Buccal mucosa is most preferred site for both local as well as systemic action. For administration of drug through mucosal route, various types of dosage forms can be prepared. Buccal films can release topical drugs with controlled and sustained effects. Buccal films have the advantage of improved patient compliance because of reduced size with a suitable thickness as compare to other delivery systems. Buccal film

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13

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

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

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14

Baratam, Srinivasa Rao, and Made Vijay Harsha. "Preparation and Characterisation of Sustained Released Dosage Form for Ketoprofen using Natural Gums." International Journal of Pharmaceutical Investigation 10, no. 1 (2020): 54–58. http://dx.doi.org/10.5530/ijpi.2020.1.10.

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15

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

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

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Paul, Sujata, Biplajit Das, and Hemanta Kumar Sharma. "A Review on Bio-Polymers Derived from Animal Sources with Special Reference to their Potential Applications." Journal of Drug Delivery and Therapeutics 11, no. 2 (2021): 209–23. http://dx.doi.org/10.22270/jddt.v11i2.4763.

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Biopolymers are naturally found material and most of the materials are made in nature during the life cycles of plants, animals, fungi and bacteria. For any pharmaceutical formulation the two main ingredients are active pharmaceutical ingredient and excipients. As excipients in any kind of dosage form, the biopolymers play a vital function. Biopolymers are pharmacologically inert ingredients formulated along with the active ingredient to increase the volume; they help in the formulating dosage form and also simultaneously can improve the physicochemical parameters of the dosage form and so are

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17

Rani, Nisha, Dhruv Dev, and D. N. Prasad. "Recent Trends in developments of Superdisintegrants: An Overview." Journal of Drug Delivery and Therapeutics 12, no. 1 (2022): 163–69. http://dx.doi.org/10.22270/jddt.v12i1.5148.

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Fast dissolving tablets are solid unit dosage forms that dissolve or disintegrate quickly in the mouth without using water. To provide this type of character in a dosage form, different excipients are required. Superdisintegrants are a class of novel agents that have emerged in recent years. Improving drug bioavailability in the pharmaceutical field is a challenge. The inclusion of superdisintegrants in the formulation enhances the formulation's efficacy. The main goal of this review article is to highlight current development in the superdisintegrants. Novel medication delivery techniques hav

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18

Sharma, Diksha, Dhruv Dev, D. N. Prasad, and Mansi Hans. "Sustained Release Drug Delivery System with the Role of Natural Polymers: A review." Journal of Drug Delivery and Therapeutics 9, no. 3-s (2019): 913–23. http://dx.doi.org/10.22270/jddt.v9i3-s.2859.

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An appropriately designed sustained release dosage form is opted to be a major goal in solving the problems which arises regarding the targeting of a drug to a specific organ or tissue and for controlling its rate of delivery to the target site. The development of oral sustained release system has proven to be a major challenge to formulation scientist due to their inability to restrain as well as localize the system at targeted areas of the gastrointestinal tract. Therefore the development of matrix type drug delivery system is promising option regarding the development of an oral sustained r

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19

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

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

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20

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

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

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Karegar-Borzi, Hossein, Mehdi Salehi, and Roja Rahimi. "Laūq." Journal of Evidence-Based Complementary & Alternative Medicine 21, no. 1 (2015): 63–70. http://dx.doi.org/10.1177/2156587215587417.

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Laūq is a pharmaceutical dosage form that had been mainly used for the treatment of various respiratory disorders in traditional Persian medicine. It is important from 2 aspects: a dosage form with efficient and optimum delivery of drugs to the respiratory tract and biological effects of its ingredients. Natural medicine in laūq has been demonstrated to act in respiratory disorders by their antitussive, antiallergic, anti-inflammatory, antioxidant, spasmolytic, and antibacterial activities. Some of these natural remedies act by most of the mentioned mechanisms such as Cydonia oblonga, Glycyrrh

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22

Yunusova, Kh M., and Sh Kh Sunnatov. "Selection of the optimal composition and technology of the recommended capsules "PROSTAD"." International Journal of Medical Sciences And Clinical Research 5, no. 3 (2025): 21–30. https://doi.org/10.37547/ijmscr/volume05issue03-05.

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In the process of searching for new effective drugs for the treatment of prostate and prostate adenoma, special attention should be paid to drugs based on natural origin. It is generally accepted that drugs obtained from natural origin are less toxic. The action of these drugs is carried out through ready-made dosage forms that are easy to use. The purpose of our work is to develop the composition and technology of an encapsulated dosage form based on Fireweed.This article presents the results of studies onthe development of tablet technology based on the recommended dry extract "Prostad". An

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23

Ramli, Rosmamuhamadani, Norashikin Salleh, Mohd Muzamir Mahat, and Sabrina M Yahaya. "Kinetic Study of Natural Anticancer Drug (Zerumbone) Release from Zeolite Y-Gelatin Hybrid for Oral Controlled Delivery." Environment-Behaviour Proceedings Journal 9, SI17 (2024): 393–98. http://dx.doi.org/10.21834/e-bpj.v9isi17.5441.

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A hybrid of zeolite Y-gelatin film as an oral dosage form for the natural anticancer drug was achieved by homogenously incorporating the drug-loaded zeolite Y into the gelatin solution. Drug ability was analyzed using computational and experimental approaches, drug encapsulation efficiency via the BET method, and possible interactions by FTIR analyses. Zerumbone released was done in both pH 1.2 and pH 7.4 mimicking the human gastrointestinal tract conditions for 24 hrs and subjected to kinetics study via suitable mathematical models to determine what governs the drug release with the results i

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Dhiman, Jasmine, Dhruv Dev, and D. N. Prasad. "Superdisintegrants: Brief Review." Journal of Drug Delivery and Therapeutics 12, no. 1 (2022): 170–75. http://dx.doi.org/10.22270/jddt.v12i1.5155.

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Oral disintegrating tablets are a new trend in novel drug delivery systems that have seen a surge in popularity in recent decades. To improve the efficacy of solid dosage forms, super disintegrants are used. This is accomplished by reducing the disintegration time, which improves the rate of drug dissolution. Disintegrants are substances or combination of substances added to a drug formulation to aid in the breaking up or disintegration of tablet or capsule content into smaller fragments that dissolve more quickly than without them. Several newer agents known as ‘Superdisintegrants’ have been

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Bondar, Dali, C. J. Lynsdale, Neil B. Milestone, N. Hassani, and A. A. Ramezanianpour. "Effect of type, form, and dosage of activators on strength of alkali-activated natural pozzolans." Cement and Concrete Composites 33, no. 2 (2011): 251–60. http://dx.doi.org/10.1016/j.cemconcomp.2010.10.021.

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Kadhim, Zahraa Mohammed, and Wedad K. Ali. "Utilization of Natural Polymer in the Preparation of Oral Jelly of Granisetron." Al Mustansiriyah Journal of Pharmaceutical Sciences 19, no. 2 (2019): 1–8. http://dx.doi.org/10.32947/ajps.v19i2.549.

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The aim of present study was to formulate and evaluate oral jellies containing granisetron (GSN). This new dosage form was designed for administration of the drug to specific aged patients (i.e. pediatric) in certain condition. GSN is an antiemetic which is usually used for the treatment of nausea and vomiting induced by radiotherapy and chemotherapy. The selection of this dosage form was based on its acceptability by pediatric population, ease of use and no need for water after taking the dose. In this study, two types of natural jellifying agents have been used in different concentrati

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Bansal, Keshav, and Meenakshi Bajpai. "Design of Solid Dosage Form using Isolated Mucilage from Cassia fistula." Research Journal of Biotechnology 16, no. 11 (2021): 51–68. http://dx.doi.org/10.25303/1611rjbt5168.

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The present study was aimed to isolate and characterize mucilage obtained from the leaves of Amaltas (Cassia fistula) and to check the binding efficiency by comparing with gum acacia. Isolation of mucilage was done by hot maceration process and investigated for various physicochemical characterization and in vitro dissolution profile to check mucilage as a binding agent. Different batches (KF1 – KF4) of paracetamol tablets of different concentration of mucilage (3%, 5%, 10% and 15% w/v) were prepared by wet granulation method. All the parameters of uncoated tablets were performed and compared

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Mishra, Manoj Kumar, Abhishek Singh, Amit Kumar Patel, Rajat Srivastava, and Krishna Kushwaha. "Recently investigated polymeric natural gums and mucilages for various drug delivery system." World Journal of Advanced Research and Reviews 6, no. 1 (2020): 050–72. https://doi.org/10.5281/zenodo.4312533.

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The use of natural excipients to deliver the bioactive agents has been hampered by the synthetic materials. However advantages offered by these natural excipients are their being non-toxic, less expensive and freely available. The performance of the excipients partly determines the quality of the medicines. The traditional concept of the excipients as any component other than the active substance has undergone a substantial evolution from an inert and cheap vehicle to an essential constituent of the formulation.  Gums are widely used natural excipients for conventional and novel dosage fo

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Gazi, Ayesha Siddiqua, Amena Begum, and Sumayeh Begum. "AN OVERVIEW ON PHARMACEUTICAL EXCIPIENTS- THEIR ROLES AND APPLICATIONS." International Journal of Pharmaceutical Sciences and Medicine 7, no. 12 (2022): 84–96. http://dx.doi.org/10.47760/ijpsm.2022.v07i12.005.

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Excipients play an important role in formulating a dosage form. These are the ingredients which along with Active Pharmaceutical Ingredients make up the dosage forms. Excipients act as protective agents, bulking agents and can also be used to improve bioavailability of drugs in some instances; the following review discusses the various types of excipients along with their uses. The objective of this paper is to indicate the ingredients that possess health effect that can be found in cosmetics and personal care products. The related paper was reviewed in terms of the chemicals that commonly ide

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Kurylenko, Viktor, Nataliia Tolstopalova, Tetiana Obushenko, Olga Sanginova, and Tetiana Dontsova. "FLUORIDE IONS REMOVAL EFFICIENCY OF NATURAL/ACTIVATED ZEOLITE AND BENTONITE SORBENTS." WATER AND WATER PURIFICATION TECHNOLOGIES. SCIENTIFIC AND TECHNICAL NEWS 36, no. 2 (2023): 27–39. http://dx.doi.org/10.20535/2218-930022023300526.

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Addressing the health concern of fluoride ions contamination in water, that cause such deceases as dental and skeletal fluorosis, requires the development of effective adsorption materials for water treatment. Our research objective was to evaluate the adsorption properties and capacities of zeolite and bentonite, sourced from Ukrainian deposits, and their acid-activated forms in relation to fluoride ions and estimate fitting this data to various adsorption models. Characterization of natural and acid-activated zeolite and bentonite sorbents was performed through X-ray diffraction to determine

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Manish, Kumar Gupta, Priya Sakshi, Singh Sudharshana, and Verma Sunil. "FORMULATION AND EVALUATIONS OF MOUTH DISSOLVING FILM USING NATURAL EXCIPIENTS." International Journal of Current Pharmaceutical Review and Research 13 (December 30, 2021): 28–37. https://doi.org/10.5281/zenodo.12667156.

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Mouth dissolving film (MDFs) is the latest oral solid dosage form because of its easy-to-useproperties. When mouth dissolving films are placed in mouth, it disintegrates and dissolveswithin a minute without consuming water or chewing. This dosage form has added advantageas it allows the medication to bypass the first pass metabolism, so bioavailability ofmedication may be enhanced. Mouth dissolving film has capability to enhance onset ofaction, lower the dosing and eliminate the fear of chocking. Over the past years, MDFs haveappeared as effective oral care products as dosage forms for deliver

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Kruk, Katarzyna, and Katarzyna Winnicka. "Alginates Combined with Natural Polymers as Valuable Drug Delivery Platforms." Marine Drugs 21, no. 1 (2022): 11. http://dx.doi.org/10.3390/md21010011.

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Alginates (ALG) have been used in biomedical and pharmaceutical technologies for decades. ALG are natural polymers occurring in brown algae and feature multiple advantages, including biocompatibility, low toxicity and mucoadhesiveness. Moreover, ALG demonstrate biological activities per se, including anti-hyperlipidemic, antimicrobial, anti-reflux, immunomodulatory or anti-inflammatory activities. ALG are characterized by gelling ability, one of the most frequently utilized properties in the drug form design. ALG have numerous applications in pharmaceutical technology that include micro- and n

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Piancita, Giga, Indriyanto -, and Duryat -. "PENGARUH DOSIS BIOSERUM TERHADAP PEMBENTUKAN GAHARU PADA Aquilaria malaccensis Lamk." Jurnal Hutan Tropis 9, no. 1 (2021): 101. http://dx.doi.org/10.20527/jht.v9i1.10482.

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Natural agarwood takes a long time to be formed in nature, therefore an improvement technique was required in order to increase the productivity of Agarwood. One of these techniques was Bioserum injection into the Aquilaria malaccensis. Bioserum is a nutritious liquid necessary for fungi to live, grow and produce the agarwood. The purpose of the research was to determine the best Bioserum dosage, the best time of Bioserum reacted, and the best interaction between the two factors in the formation of agarwood. Factorial Completely Randomized Design (FCRD) with two factors, namely the dosage of B

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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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Lupitko, E. M., E. F. Stepanova, and D. A. Bagaev. "Prospects for the development of a mild dosage form based on pumpkin seed oil (overview)." Farmacevticheskoe delo i tehnologija lekarstv (Pharmacy and Pharmaceutical Technology), no. 2 (April 10, 2025): 35–53. https://doi.org/10.33920/med-13-2502-06.

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Pumpkin seed oil, which contains a large amount of biologically active substances, is a valuable product of natural origin. The pronounced activity of carotenoids in pumpkin oil allows us to consider them as the main active substances (in a mild dosage form) that have a wound-healing effect. Oleogel is a romising mild dosage form for vegetable oils, as it has a number of significant advantages over ointments or creams. The optimal thickener for vegetable oils is aerosil, which makes it possible to obtain stable oleogels with good rheological characteristics. Purpose of the work: to summarize t

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Mustafa, Muhammad Abid, Nasira Saif ur Rehman, Asad Majeed Khan, et al. "Formulation and in vitro Evaluation of Natural Polymer Based Albendazole Gummies: A Novel Pediatrics Dosage Form." Journal of Young Pharmacists 15, no. 3 (2023): 478–84. http://dx.doi.org/10.5530/jyp.2023.15.63.

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Patel, Ojas, and Mona Patel. "DEVELOPMENT AND EVALUATION OF POLY-HERBAL SYRUP FROM NATURAL INGREDIENTS HAVING EXPECTORANT AND ANTIPYRETIC ACTIVITY." International Journal of Research in Ayurveda and Pharmacy 12, no. 3 (2021): 46–51. http://dx.doi.org/10.7897/2277-4343.120372.

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Ayurvedic formulations are mainly administered by oral route and most of the orally administered Ayurvedic formulations belong to liquid dosage form of drug or drug combination. However, Herbal products have to fulfil legal requirements with regards to quality including stability testing. Herbal Syrup is commonly used and popular dosage form which is used to cure cough, cold and fever because it having ease of patients compliance. In present study, Prepared Herbal Syrup contain Ginger macerated honey base and also Tulsi, liquorice, neem, amla, cinchona, fennel, peppermint, turmeric, brahmi, cl

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S., Divakar* K. Shanthini. "Formulation and Evaluation of Trigonella foenum-graecum l. loaded Nanostructured Lipid Carrier based Buccal Patch by using Natural oil." International Journal of Pharmaceutical Sciences 2, no. 7 (2024): 706–24. https://doi.org/10.5281/zenodo.12730715.

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Nano structured lipid carrier(NLC) are the 2nd generation lipid Nanoparticle formulated using <em>Trigonella foenum-graecum l.</em> loaded into NLC as Buccal patch as a dosage form to enhance the efficiency of the drug for the treatment of Hyperglycemia. Using Stearic acid and Soybean oil as lipid phase and Span 60 with water as aqueous phase mixed together completely using magnetic stirrer to form a emulsion. Formed NLC emulsion loaded into the buccal patch as a dosage form. Among the formulations N1 to N8, formulation N4 consider as the best with the drug release of 97%. Formulation N4 incor

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Norashikin Salleh, Mohd Muzamir Mahat, Sabrina M. Yahaya, and Rosmamuhamadani Ramli. "Kinetic and Mechanism of Zerumbone Release from Cross-linked Gelatin-Zeolite Y Hybrid for Oral Anticancer Drug Delivery." Journal of Advanced Research in Fluid Mechanics and Thermal Sciences 115, no. 1 (2024): 181–92. http://dx.doi.org/10.37934/arfmts.115.1.181192.

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A hybrid of zeolite Y-gelatin film as an oral dosage form for the natural anticancer drug was achieved by homogenously incorporating the drug-loaded zeolite Y into the gelatin solution. Drug ability was analyzed using computational and experimental approaches, drug encapsulation efficiency via the BET method, and possible interactions by FTIR analyses. Zerumbone released was done in both pH 1.2 and pH 7.4 mimicking the human gastrointestinal tract conditions for 24 hrs and subjected to kinetics study via suitable mathematical models to determine what governs the drug release with the results i

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Norashikin Salleh, Mohd Muzamir Mahat, Sabrina M. Yahaya, and Rosmamuhamadani Ramli. "Kinetic and Mechanism of Zerumbone Release from Cross-linked Gelatin-Zeolite Y Hybrid for Oral Anticancer Drug Delivery." Journal of Advanced Research in Micro and Nano Engieering 18, no. 1 (2024): 32–43. http://dx.doi.org/10.37934/armne.18.1.3243.

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A hybrid of zeolite Y-gelatin film as an oral dosage form for the natural anticancer drug was achieved by homogenously incorporating the drug-loaded zeolite Y into the gelatin solution. Drug ability was analyzed using computational and experimental approaches, drug encapsulation efficiency via the BET method, and possible interactions by FTIR analyses. Zerumbone released was done in both pH 1.2 and pH 7.4 mimicking the human gastrointestinal tract conditions for 24 hrs and subjected to kinetics study via suitable mathematical models to determine what governs the drug release with the results i

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Opryshko, V. I., V. I. Мamchur, D. S. Nosivets, A. V. Prokhach, and A. S. Kurt-Ametova. "Effective, safe and rational pharmacotherapy of endogenic progesterone deficiency." Reproductive health of woman 1 (February 26, 2021): 21–25. http://dx.doi.org/10.30841/2708-8731.1.2021.229705.

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Today, the most frequent complication of pharmacotherapy is an allergic reaction, the so-called drug or drug allergy. An allergic reaction can be caused both by the active ingredients and by the excipients included in the composition of the drug to provide a certain dosage form and its physicochemical properties. Vaginal progesterone preparations are characterized by a large variety of dosage forms: gels, tablets and gelatin capsules for intravaginal administration. It is known that the safety and efficacy of pharmacotherapy depend on the active substance, the dosage form, and the base of the

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

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

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Gómez-Llorente, Héctor, Isabel Fernández-Segovia, Édgar Pérez-Esteve, et al. "Immobilization of Natural Antimicrobial Compounds on Food-Grade Supports as a New Strategy to Preserve Fruit-Derived Foods." Foods 12, no. 10 (2023): 2060. http://dx.doi.org/10.3390/foods12102060.

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The use of natural antimicrobials in the food industry is being proposed as an eco-friendly postharvest technology to preserve fruit-derived foods. In this context, this systematic review aims to describe and discuss the application of naturally occurring antimicrobial compounds in the processing of fruit-derived foods by the PRISMA methodology. In a first step, the use of free natural antimicrobials was investigated as an approach to identify the main families of bioactive compounds employed as food preservatives and the current limitations of this dosage form. Then, the use of immobilized an

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Kumar Raja Jayavarapu, Praveen Kumar Dassari, Malleli Bhavya Sai Kumari, and Yalam Saranya. "Formulation and evaluation of dosage form of fast dissolving oral film of Rofecoxib." World Journal of Biology Pharmacy and Health Sciences 19, no. 1 (2024): 371–81. http://dx.doi.org/10.30574/wjbphs.2024.19.1.0449.

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Rofecoxib is utilized for the treatment of osteoarthritis, rheumatoid joint inflammation, intense torment in grown-ups, and essential dysmenorrhea, just as intense therapy of headache assaults with or without emanations. Rofecoxib is strong. This compound has a place with the stilbenes. These are natural mixes containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are acquired from the normal phenylpropene (C6-C3) skeleton building block. The presentation of at least one hydroxyl gathering to a phenyl ring leads to stilbenoids. Rofecoxib has a half-existence of 17 hours and its mean o

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Kumar, Raja Jayavarapu, Kumar Dassari Praveen, Bhavya Sai Kumari Malleli, and Saranya Yalam. "Formulation and evaluation of dosage form of fast dissolving oral film of Rofecoxib." World Journal of Biology Pharmacy and Health Sciences 19, no. 1 (2024): 371–81. https://doi.org/10.5281/zenodo.13789899.

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Rofecoxib is utilized for the treatment of osteoarthritis, rheumatoid joint inflammation, intense torment in grown-ups, and essential dysmenorrhea, just as intense therapy of headache assaults with or without emanations. Rofecoxib is strong. This compound has a place with the stilbenes. These are natural mixes containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are acquired from the normal phenylpropene (C6-C3) skeleton building block. The presentation of at least one hydroxyl gathering to a phenyl ring leads to stilbenoids. Rofecoxib has a half-existence of 17 hours and its mean o

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Čanji-Panić, Jelena, Nemanja Todorović, Ana Stjepanović, and Mladena Lalić-Popović. "The potential of natural products use in fused deposition modeling 3D printing of pharmaceutical dosage forms." Arhiv za farmaciju 72, no. 6 (2022): 621–36. http://dx.doi.org/10.5937/arhfarm72-40155.

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In recent years, the interest in 3D printing of medicines has increased due to many advantages of this technology, such as flexibility of the dose and dosage form of the printed product. Fused deposition modeling (FDM) is one of the most popular 3D printing technologies in the pharmaceutical field, due to its low cost and simplicity. The subject of this review is the potential use of natural products as biodegradable and biocompatible materials with good safety profiles in FDM 3D printing of pharmaceuticals. Natural products such as alginate, chitosan and starch have already been employed as e

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Gnanasekaran John Selvaraj, Arul Balasubramanian, and Kothai Ramalingam. "A Mini Review on Mucoadhesion." International Journal of Research in Pharmaceutical Sciences 11, no. 3 (2020): 3521–27. http://dx.doi.org/10.26452/ijrps.v11i3.2505.

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The concept of mucoadhesion was started in early 1980’s with the aim of controlled delivery of drugs. Mucoadhesion is simply defined as the adhesion between two materials, in which one is the mucosal surface and the another one is the mucoadhesive dosage form. In the recent decades, mucoadhesive drug delivery system draw the attention in the gastroretentive delivery system. Mucoadhesive drug delivery systems interact with the mucus layer covering the mucosal epithelial surface, and mucin molecules and increase the residence time. Mucoadhesive dosage forms are designed to increase the retention

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Sonar, Shivani, Sheetal Gondkar, and Ravindranath B. Saudagar. "Liquid Filled Hard Gelatin Capsule." Journal of Drug Delivery and Therapeutics 9, no. 3-s (2019): 832–35. http://dx.doi.org/10.22270/jddt.v9i3-s.2794.

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Novel dosage forms emerges more and more in recent years. One of them is liquid-filled hard gelatin capsules, which have gelatin or the hydroxypropyl methyl cellulose (HPMC) as capsule shell. The liquid-filled hard gelatin capsule is gradually getting attention because of its new-concept dosage form design, which bring liquid drugs by solid form. The paper mostly presents application, pharmaceutical manufacturing, quality assessment, vision of liquid-filled hard gelatin capsules and emphases on the application and pharmaceutical manufacturing of liquid-filled capsule. It is recommended that th

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Chakraborty, Santanu, Madhusmruti Khandai, Manami Dhibar, Shikha Yadav, and Honey Kumari. "Isolation and Characterization of Dillenia Fruit Mucilage: A Novel Polymer for Microspheric Delivery of Losartan Potassium." Drug Delivery Letters 10, no. 4 (2020): 314–25. http://dx.doi.org/10.2174/2210303110999200802030342.

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Objective: The present investigation was aimed to isolate, characterize and establish a natural polymer obtained from partially ripe and fresh fruits of Dillenia indica and its utility to deliver losartan potassium in a sustained manner from microspheric macromolecular dosage form. Methods: All the microspheres were prepared by ionotropic gelation technique and investigated for various physico-chemical parameters along with in-vitro drug release studies to optimize the concentration of algino-Dillenia polymeric blend required to develop twice daily sustained release dosage form of losartan pot

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Anjali, Joshi* and Ganesh Kumar. "FAST DISSOLVING THIN STRIPS: AN EMERGING WAY FOR ORAL DRUG DELIVERY." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 01 (2018): 429–38. https://doi.org/10.5281/zenodo.1160888.

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Various pharmaceutical dosage form are present in the market but all of the dosage forms possess some drawback most common is patient incompliance which is seen in all age groups. So from last few years focus is done on developing such dosage form which enhances safety, efficacy and patient compliance. In this manner, in late 1970 fast-dissolving drug delivery system came in existence which includes Fast dissolving tablets and fast dissolving thin strips means those dosage form which dissolves in the oral cavity when came in contact with saliva. Fast dissolving thin strips have various advanta

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