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1 of 40
Prepared By
Miss. Mane Deshmukh P.P.
Guided By
Mrs. Barhate A.N.
SVPM’S COLLEGE OF PHARMACY
MALEGAON (BK)
1
 Introduction
 Definition
 Formation of liposome
 Structural components
 Composition of liposomes
 Classifications
 Advantages & disadvantages
 Preparation methods
 Limitations of liposomes technology
 Characterization of liposomes
 Applications
 Marketed Preparations
 References
2
INTRODUCTION
3
Definition 1,16:-
“Liposomes are defined as structure consisting of
one or more concentric spheres of lipid bilayers separated by
water or aqueous buffer compartments”.
4
FORMATION OF LIPOSOME s 19,20 :-
5
STRUCTURALCOMPONENT 3,12-13:-
6
 Phospholipids
 Sphigolipids
 Cholesterols
 Polymer material
 Polymer lipids Bearing
 Cationic lipids
 Other substance
7
CLASSIFICAT ION 8-18 :-
8
9
Classes of Liposomes 12 :-
10
11
 It should be biodegradable, biocompatible, and
flexible. It can carry both water and lipid soluble
drugs.
 The drugs can be stabilized from oxidation.
 It should be improve the protein stabilization.
 It provides controlled hydration,sustained release,
targeted drug delivery or site specific drug
delivery.
 Stabilization of entrapped drug from hostile
environment.
 Alter pharmacokinetics and pharmacodynamics
of drugs.
 It can be administered through various routes.
 It can incorporate micro and macro molecules
Advantages 10-18 :-
12
 It has stability
 It has solubility
 It has short half life
 The phospholipids undergoes
oxidation, hydrolysis
 Leakage and fusion
 It is high production cost
 Some time allergic reactions
may occur to liposomal
constituents
Disadvantages 10-18 :-
13
PREPARATION METHODS 1-8,12-16 :-
14
15
2
16
MECHANICAI DISPERSIONMETHOD:
17
18
FREEZE THAWSONICATION(FTS):-
19
SOLVANT DISPERSION METHOD:-
20
21
22
LIMITATIONS OF LIPOSOMES TECHNOLOGY (15) :-
23
24
25
26
27
28
29
30
CHARACTERIZATION 11-13:-
31
32
APPLICATIONS:-
33
34
MARKETED PREPRATION21-22 :-
35
1) Aulton ME. Pharmaceutics-The science of dosage
form design, 2002, 2nd edit.
2) Banker S. Modern pharmaceutics, 2009, vol.121, 4th
edi., 275
3) Vyas S.P. & Khar R.K. “Targeted & controlled drug
delivery : Novel carrier system”. CBS publishers and
distributors, 2007.
4) Ansels ,Pharmaceutical dosage forms& Drug
delivery system,8th edi.
36
5) Lidgate DM, Felgner PL, In vitro and in vivo studies
evaluating a liposome system for drug solubilisation. Pharm
Res 1988; 5: 759–764.
6) P, Bilandi A, Akanksha M, Kapoor B, Seth GL,
BihaHimanshu A, Sitasharan P, Singhai AK: Liposomes as
drug carriers. Int J Pharm Liposomes System 2011,
2(7):945–951.
7) Kataria S, Sandhuni SD:Stealth liposomes: a review. Int J
Res Art Pharm, 2011, 2(5):1534–1538
8) Jessy S,Vinay B, Novel delivary system.Int.j pharm bio sci
2013 Jan(1):150-160
37
9) Barain, H. & Montazer, M,A Review on Applications
of Liposomes in Textil Processing. of Liposome Res,
2008 ;18 (3) 249-262
10) Anna J,Liposomes,J Pharm Sci. & Res. 2013,5(9)
181- 183
11)Patel N,Panda S,Liposomes drug delivary system.J
Pharm Sci Bio Res 2012;2(4):169-175
12) Thulasiramaraju T,Sudhakar b, Liposomes.A Novel
drug delivary system.Int J Bio Pharm 2012;3(1):5-16
13) Kulkarni p,Yadav j. Liposomes.A Novel drug
delivary system.Int J Curr Peper Res2011 ;3(2),10
38
14) Harashima, H., Sakata, K., Funato, K., Kiwada, H.,
1994.Enhanced hepatic uptake of liposomes through
complement activation depending on the size of
liposomes.Pharm. Res. 11,402-406.
15) Sharma A.Liposome in drug delivery progress and
limitation. Int j pharm. 1997; 154;123-140.
16) Abdus S. Liposome drug delivery system
an update review. Current drug delivery.2007; 4; 297-
305
17) Mansoori and Agrawal, Liposome drug delivery
system ,Int J Art Res Pharm Bio, 2012; Vol.2 (4):453-
464
39
18) Shashi K., Satinder K, Bharat P. A Complete
Review on Liposomes. Int Res J Pharm 2012;3(7)
10-16
19) Lasic D. Mechanism of liposome formation
Journal of liposome research. 1995; 5(3); 431-441.
20) Lasic D. Mechanism of liposome formation
.Journal of liposome research.1995; 5(3); 431-441.
21)www.slideshare.com
22) www.authorstream.com
40

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Liposomes ppt

  • 1. Prepared By Miss. Mane Deshmukh P.P. Guided By Mrs. Barhate A.N. SVPM’S COLLEGE OF PHARMACY MALEGAON (BK) 1
  • 2.  Introduction  Definition  Formation of liposome  Structural components  Composition of liposomes  Classifications  Advantages & disadvantages  Preparation methods  Limitations of liposomes technology  Characterization of liposomes  Applications  Marketed Preparations  References 2
  • 4. Definition 1,16:- “Liposomes are defined as structure consisting of one or more concentric spheres of lipid bilayers separated by water or aqueous buffer compartments”. 4
  • 5. FORMATION OF LIPOSOME s 19,20 :- 5
  • 7.  Phospholipids  Sphigolipids  Cholesterols  Polymer material  Polymer lipids Bearing  Cationic lipids  Other substance 7
  • 9. 9
  • 11. 11
  • 12.  It should be biodegradable, biocompatible, and flexible. It can carry both water and lipid soluble drugs.  The drugs can be stabilized from oxidation.  It should be improve the protein stabilization.  It provides controlled hydration,sustained release, targeted drug delivery or site specific drug delivery.  Stabilization of entrapped drug from hostile environment.  Alter pharmacokinetics and pharmacodynamics of drugs.  It can be administered through various routes.  It can incorporate micro and macro molecules Advantages 10-18 :- 12
  • 13.  It has stability  It has solubility  It has short half life  The phospholipids undergoes oxidation, hydrolysis  Leakage and fusion  It is high production cost  Some time allergic reactions may occur to liposomal constituents Disadvantages 10-18 :- 13
  • 15. 15
  • 16. 2 16
  • 18. 18
  • 21. 21
  • 22. 22
  • 23. LIMITATIONS OF LIPOSOMES TECHNOLOGY (15) :- 23
  • 24. 24
  • 25. 25
  • 26. 26
  • 27. 27
  • 28. 28
  • 29. 29
  • 30. 30
  • 32. 32
  • 34. 34
  • 36. 1) Aulton ME. Pharmaceutics-The science of dosage form design, 2002, 2nd edit. 2) Banker S. Modern pharmaceutics, 2009, vol.121, 4th edi., 275 3) Vyas S.P. & Khar R.K. “Targeted & controlled drug delivery : Novel carrier system”. CBS publishers and distributors, 2007. 4) Ansels ,Pharmaceutical dosage forms& Drug delivery system,8th edi. 36
  • 37. 5) Lidgate DM, Felgner PL, In vitro and in vivo studies evaluating a liposome system for drug solubilisation. Pharm Res 1988; 5: 759–764. 6) P, Bilandi A, Akanksha M, Kapoor B, Seth GL, BihaHimanshu A, Sitasharan P, Singhai AK: Liposomes as drug carriers. Int J Pharm Liposomes System 2011, 2(7):945–951. 7) Kataria S, Sandhuni SD:Stealth liposomes: a review. Int J Res Art Pharm, 2011, 2(5):1534–1538 8) Jessy S,Vinay B, Novel delivary system.Int.j pharm bio sci 2013 Jan(1):150-160 37
  • 38. 9) Barain, H. & Montazer, M,A Review on Applications of Liposomes in Textil Processing. of Liposome Res, 2008 ;18 (3) 249-262 10) Anna J,Liposomes,J Pharm Sci. & Res. 2013,5(9) 181- 183 11)Patel N,Panda S,Liposomes drug delivary system.J Pharm Sci Bio Res 2012;2(4):169-175 12) Thulasiramaraju T,Sudhakar b, Liposomes.A Novel drug delivary system.Int J Bio Pharm 2012;3(1):5-16 13) Kulkarni p,Yadav j. Liposomes.A Novel drug delivary system.Int J Curr Peper Res2011 ;3(2),10 38
  • 39. 14) Harashima, H., Sakata, K., Funato, K., Kiwada, H., 1994.Enhanced hepatic uptake of liposomes through complement activation depending on the size of liposomes.Pharm. Res. 11,402-406. 15) Sharma A.Liposome in drug delivery progress and limitation. Int j pharm. 1997; 154;123-140. 16) Abdus S. Liposome drug delivery system an update review. Current drug delivery.2007; 4; 297- 305 17) Mansoori and Agrawal, Liposome drug delivery system ,Int J Art Res Pharm Bio, 2012; Vol.2 (4):453- 464 39
  • 40. 18) Shashi K., Satinder K, Bharat P. A Complete Review on Liposomes. Int Res J Pharm 2012;3(7) 10-16 19) Lasic D. Mechanism of liposome formation Journal of liposome research. 1995; 5(3); 431-441. 20) Lasic D. Mechanism of liposome formation .Journal of liposome research.1995; 5(3); 431-441. 21)www.slideshare.com 22) www.authorstream.com 40