Syllabus

JNTUK B. Tech Controlled release & Novel Drug Delivery Systems for R13 Batch.

JNTUK B.Tech Controlled release & Novel Drug Delivery Systems gives you detail information of Controlled release & Novel Drug Delivery Systems R13 syllabus It will be help full to understand you complete curriculum of the year.

UNIT – I : Controlled and sustained release: Factors to be considered – Principles involved in their design – regulatory considerations.
LO : To understand Controlled and sustained release: Factors to be considered – Principles involved in their design – regulatory considerations.

UNIT – II : Oral Control Drug Delivery Systems: Fundamentals, Dissoultion Controlled, Diffusion Controlled, Ion Exchange Resins, Osmotic based systems, pH Independent Systems and altered density systems.
LO : To understand fundamentals, Dissoultion Controlled, Diffusion Controlled, Ion Exchange Resins, Osmotic based systems, pH Independent Systems and altered density systems.

UNIT – III : Transdermal Drug Delivery Systems: Fundamentals, types of TDDS, Materials Employed and Evaluation of TDDS.
LO : To understand fundamentals, types of TDDS, Materials Employed and Evaluation of TDDS.

UNIT – IV : Mucoadhesive Delivery Systems: Mechanism of bioadhesion, mucoadhesive materials, forumulation and evaluation of mucoadhesive-based systems.
LO : To understand mechanism of bioadhesion, mucoadhesive materials, forumulation and evaluation of mucoadhesive-based systems.

UNIT – V : Targeted Drug Delivery Systems: Fundamentals and applications, formulation and evaluation of liposomes, resealed erythrocytes and nano particles.
LO : To understand fundamentals and applications, formulation and evaluation of liposomes, resealed erythrocytes and nano particles.

UNIT – VI : Study of polymers for controlled release – Classification, study of biodegradable polymers & hydrogels – their applications.
LO : To understand classification, study of biodegradable polymers & hydrogels – their applications.

TEXT BOOKS

  • N.K. Jain, Control Drug Delivery Systems by
  • Y.Anjaneyulu&Maraiah, Quality Assurance & Quality Management in Pharmaceutical Industry.
  • L. Lachman, H.A, Lieberman and J.L. Kanig, Theory & Practice of industrial pharmacy by, Lea &Febieger, Philadelphia Latest Edn.
  • Shobhan Rani Hiremath Text Book of Industrial Pharmacy.

REFERENCES

  • Leon ShargelIsadoreKanfer, Generic Drug Product Development, Solid Oral Dosage Forms, Marcel Dekker.
  • Sagarian& MS Balsam, Cosmetics Sciences &Technology.Vol.1, 2 & 3
  • Lippincott Williams and Wilkins, Remington Pharmaceutical Sciences
  • E.A Rawlkins, Bentley’s Text Book of Pharmaceutics, ELBS publ
  • HC Ansel, Introduction to Pharmaceutical Dosage forms
  • S.H. Willing, M.M Tucherman and W.S. Hitchings IV, Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control, Marcel Dekker, Inc., New York
  • Gilbert S. Banker and Christopher T Rhodes, Modern Pharmaceutics, IVthed, marcel dekker, USA, 2005.
  • YiewChien, novel drug delivery systems, 2nded, marcel dekker 2003.
  • Robert. A. Nash, Pharmaceutical Process Validation, 3rd Ed Marcel Dekker, 2003.
  • Good Manufacturing Practices – Schedule M, Read with The Drugs And Cosmetic Rules 1945.
  • M.E. Aulton, Pharmaceuitcs- The science of Dosage form Design 2nded. 12. AukunuruJithan, Oral Drug Delivery Technology.

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