Laboratory Manual of Herbal Drug Technology

Laboratory Manual of Herbal Drug Technology

Author: Mr. Vijay D. Havaldar

Publisher: Trinity Publishing House, Satara

Published: 2024-02-16

Total Pages: 112

ISBN-13: 8196569440

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We are very pleased to put forth the 'Herbal Drug Technology'. This manual is prepared as per PCI B. Pharm course regulations 2014 and is divided into six sections i. e. Preliminary phytochemical screening, Determination of alcohol contents in Ayurvedic formulations, Evaluation of natural origin excipients, Preparation and evaluation of herbal formulations, Monograph analysis of herbal drugs from recent Pharmacopoeias and Determination of chemical constituent contents. The various techniques are used for phytochemical screening of aqueous extract of crude drugs and determination of chemical constituents contents in crude drugs. The manual includes experiments through which students learn to prepare and evaluate various herbal formulations and analyze the individual monographs from recent pharmacopoeias. This manual is designed for 'outcome-based education' and each experiment is arranged in a uniform way such as practical significance, practical outcomes (PrOs) and its mapping with course outcomes, theory, resources used, procedure, precautions, observations, result, conclusion, references, and synopsis questions. Each experiment offers an opportunity to perform practical work, allowing students to gain proficiency in effectively managing equipment, handling glassware, chemicals and staining agents/ reagents, and writing conclusion. In addition, questions are provided at the end of the experiments to enhance students' knowledge, which will be beneficial for them as they pursue higher studies. During the laboratory period you will have to multitask, while you are doing experiment. It is essential to document properly what you do and what you observe while doing the practical. Always plan your work ahead and think about what you are doing, why you are doing it, what is happening and what you can conclude from your experiment. We acknowledge the help and co-operation extended by various persons in bringing out this manual. We are highly indebted to the authors of various books and articles mentioned in the reference which became a major source of information for writing this manual. We also thank the publishers, designers and printers who graciously worked hard to publish this manual in time. We hope that this manual will assist students in understanding concepts, principles, and performing procedures. We wish you all the best!"


Indian Pharmacopoeia 2014 (4 Vol Set)

Indian Pharmacopoeia 2014 (4 Vol Set)

Author: Indian Pharmacopoeia Commission

Publisher:

Published: 2013-11-01

Total Pages:

ISBN-13: 9789381238073

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The seventh edition of the Indian Pharmacopoeia (IP 2014) is published by the Indian Pharmacopoeia Commission (IPC) on behalf of the Government of India, Ministry of Health & Family Welfare. The Indian Pharmacopoeia (IP) is published in fulfilment of the requirements of the Drugs and Cosmetics Act, 1940 and Rules thereunder. It prescribes the standards for drugs produced and/or marketed in India and thus contributes in the control and assurance of the quality of the medicines. The standards of this pharmacopoeia are authoritative and legally enforceable. It intends to help in the licensing of manufacturing, inspection and distribution of medicines. IP is published in continuing pursuit of the mission of IPC to improve the health of the people through ensuring the quality, safety and efficacy of medicines. The Commission has been receiving significant inputs from regulatory, industrial houses, academic institutions, national laboratories, individual scientists and others. Publication of IP at regular and shorter intervals is one of the main mandates of the Commission. The seventh edition of Indian Pharmacopoeia is published in accordance with the principles and designed plan decided by the Scientific Body of the IPC. To establish transparency in setting standards for this edition the contents of new monographs, revised appendices and other informations have been publicized on the website of the IPC, besides following conventional approach of obtaining comments. The feedback and inputs were reviewed by the relevant Expert Committee to ensure the feasibility and practicability of the standards and methods revised. The principle of "openness, justice and fairness" is kept in mind during compiling and editing the contents of this edition. The Indian Pharmacopoeia 2014 is presented in four volumes. The scope of the Pharmacopoeia has been extended to include products of biotechnology, indigenous herbs and herbal products, veterinary vaccines


Pharmaceutics-I (Theory)

Pharmaceutics-I (Theory)

Author: Dr Suresh Kumar Thakur

Publisher: Crown Publishng

Published: 2024-03-12

Total Pages: 205

ISBN-13: 8196736509

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'Pharmaceutics-I' is a book on pharmaceutical experiments for First Semester B.Pharm students. It has relevant features like tables, diagrams, uses of ingredients. The author has also included viva questions after each practical. The information given is duly updated in accordance with the Based on syllabus prescribed by PCI Course Regulations 2014 .The students and teachers, alike, will find the book useful. It has covered topics like syrups, elixirs,solutions, suspensions, emulsions, powders and granules, suppositories, semisolids and gargles and mouthwashes, etc. It is different from other books as it is based on actual experiments carried out by the author.


The British Pharmacopoeia, 1864 to 2014

The British Pharmacopoeia, 1864 to 2014

Author: Anthony C. Cartwright

Publisher: Routledge

Published: 2016-03-09

Total Pages: 281

ISBN-13: 1317039785

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The British Pharmacopoeia has provided official standards for the quality of substances, medicinal products and articles used in medicine since its first publication in 1864. It is used in over 100 countries and remains an essential global reference in pharmaceutical research and development and quality control. This book explores how these standards have been achieved through a comprehensive review of the history and development of the pharmacopoeias in the UK, from the early London, Edinburgh and Dublin national pharmacopoeias to the creation of the British Pharmacopoeia and its evolution over 150 years. Trade in medicinal substances and products has always been global, and the British Pharmacopoeia is placed in its global context as an instrument of the British Empire as it first sought to cover the needs of countries such as India and latterly as part of its role in international harmonisation of standards in Europe and elsewhere. The changing contents of the pharmacopoeias over this period reflect the changes in medical practice and the development of dosage forms from products dispensed by pharmacists to commercially manufactured products, from tinctures to the latest monoclonal antibody products. The book will be of equal value to historians of medicine and pharmacy as to practitioners of medicine, pharmacy and pharmaceutical analytical chemistry.


Pharmaceutical Dosage Forms and Drug Delivery Systems

Pharmaceutical Dosage Forms and Drug Delivery Systems

Author: Howard C. Ansel

Publisher: Lippincott Williams & Wilkins

Published: 1999

Total Pages: 0

ISBN-13: 9780683305722

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This work covers the entire scope of pharmaceutics, from the basics of drug dosage and routes of administration to the finer points of drug discovery, drug product development, legislation and regulations governing quality standards and product approval for marketing.