The principles and procedures involved in the determination of official compounds in IP with the following analytical techniques. A detailed study of the principles and procedures involved in the quantification of the following organic functional groups. Principles and procedures involved in the use of the following reagents in the determination of official pharmaceutical dosage forms in IP.
The course includes the use of instrumental analysis in the determination of pesticides in various food products. Course outcome: Upon completion of this course, the student will be able to understand various analytical techniques in determining. Course objective: The course is intended to transfer knowledge in the field of pharmaceutical analysis.
The various modern analytical techniques such as UV-Visible, IR, NMR, Mass, GC, HPLC, different chromatographic methods and other important topics are taught to enable the students to understand the principles involved in the determination of different bulk drugs and their formulation. understand and apply. . Course outcome: Considerable knowledge will be acquired by the students in the Modern Analytical Techniques and can apply the theories in the Analysis of various bulk drugs and their formulations. Course Objective: The topics present in the pharmaceutical management are very useful for the students in personality development to become a perfect pharmaceutical professional.
The topics will help students to be exposed to processes involved in the production of herbal cosmetics, including the preparation of skin and hair care herbal products and their evaluation. Course Objectives: This topic covers various hyphenated analytical instrumental techniques for the identification, characterization and quantification of drugs. Course Outcome: The study of this subject builds confidence in the minds of the students to develop and formulate high quality pharmaceutical products.
Course Objectives: This course is designed to provide detailed knowledge about the importance of drug analysis in biological matrices. Extraction of drugs and metabolites from biological matrices: General need, principle and procedure involved in bianalytical methods such as protein precipitation, liquid-liquid extraction and solid phase extraction and other novel sample preparation approaches. Course Objective: Students will study various drug screening techniques for various pharmacological activities and guidelines for animal treatment and human and animal ethics for drug screening.
Course Outcome: The expected outcomes are that students will know how to handle animals and will know about different drug screening techniques for different pharmacological activities, guidelines and regulations for screening new drug molecules in animals. Course Objective: These topics are designed to provide a specialized knowledge to preserve the properties of drugs and dosage forms during production storage and shelf life. Analysis of drugs from biological samples including, selection of biological sample, extraction of drugs with different methods such as LLE, SPE and membrane filtration.
Course outcomes – The students should be able to choose the right kind of materials, be able to develop nanoformulations with appropriate technologies, evaluate the product related test and for identified diseases.
Introduction to Nanotechnology
Course objective - To develop expertise related to the suitability and evaluation of nanomaterials, able to apply the properties in the fabrication of nanopharmaceuticals, evaluate the intensity of dosage forms and availability for targeting and controlled delivery.
Synthesis of Nanomaterials
Biomedical applications of Nanotechnology a) Nanotechnology products used for in vitro diagnostics
Performance evaluation of cosmetic products is included for better understanding of the equipment used for this purpose in the cosmetic industry. Herbal Medicines - Toxicity and Regulation: Herbal versus Conventional Medicines, Efficacy of Herbal Medicines, Validation of Herbal Therapies, Pharmacodynamic and Pharmacokinetic Issues. Adulteration and deterioration: Introduction, types of adulteration/substitution of herbal medicines, causes and measures of adulteration, sampling procedures, determination of foreign substances, DNA fingerprinting techniques in the identification of medicines of natural origin, heavy metals, pesticide residues, phototoxin and microbial contamination in herbal formulations.
Regulatory Requirements for Establishing Herbal Medicines Industry: Global Marketing Management, Indian and International Patent Laws as Applicable Herbal Medicines and Natural Products and its Protocol. Testing of natural products and drugs: effect of herbal medicine on clinical laboratory tests, screening of adulterants using modern analytical instruments, regulation and dispensing of herbal medicines, stability testing of natural products, protocol. Monographs of Herbal Medicines: Study of Monographs of Herbal Medicines and Comparative Research in IP, USP, Ayurvedic Pharmacopoeia, American Herbal Pharmacopoeia, British Herbal Pharmacopoeia, Siddha and Unani Pharmacopoeia, WHO Guidelines for Quality Assessment of Herbal Medicines.
Herbal Medicine-Drug Interaction: WHO and AYUSH Guidelines for Safety Monitoring of Herbal Medicines, Spontaneous Reporting Schemes for Biologic Drug ADRs, Bio-Drug-Drug and Bio-Drug-Food Interactions with Appropriate Examples. Evaluation of cosmetic products: Determination of acid value, ester value, saponification value, iodine value, peroxide value, rancidity, moisture, ash, volatile substances, heavy metals, fineness of powder, density, viscosity of cosmetic raw materials and finished products. Examination of the quality of raw materials and general methods of analysis of raw materials used in cosmetic manufacturing as per BIS.
Indian Standard Specification laid down for sampling and testing of various cosmetics in finished forms such as baby care products, skin care products, dental products, personal hygiene preparations, lipsticks. JAWAHARLAL NEHRU TECHNOLOGICAL UNIVERSITY HYDERABAD I Year – II Sem M. Determination of Bulk Drugs and Formulations by UV-Visible, HPLC, GC etc. Determination of Chlorides and Sulphates by Nephelo-Tubmidimetry 5. Determination of Moisture Content, Ampicillin, Sorbitol, Ampicill etc.
