Microemulsion là gì

Silicone Microemulsion Soft And.

Kết quả: 6, Thời gian: 0.0285

1. Fleece D, Gaughan JP, Aronoff SC. Griseofulvin versus terbinafine in the treatment of tinea capitis: A meta-analysis of randomized, clinical trials. Pediatrics. 2004;114[5]:1312–5. doi: 10.1542/peds.2004-0428. [PubMed] [CrossRef] [Google Scholar]

2. Moghimipour E, Salimi A, Hassanvand S. Permeability assessment of griseofulvin microemulsion through rat skin. Int J Pharm Chem Biol Sci. 2013;3[4]:1061–5. [Google Scholar]

3. Asahina A, Tada Y, Nakamura K, Tamaki K. Griseofulvin has a potential to modulate the expression of cell adhesion molecules on leukocytes and vascular endothelial cells. Int Immunopharmacol. 2001;1[1]:75–83. doi: 10.1016/S0162-3109[00]00266-6. [PubMed] [CrossRef] [Google Scholar]

4. Shishu A, Aggarwal N. Preparation of hydrogels of griseofulvin for dermal application. Int J Pharm. 2006;326[1-2]:20–4. doi: 10.1016/j.ijpharm.2006.07.001. [PubMed] [CrossRef] [Google Scholar]

5. Fujioka Y, Metsugi Y, Ogawara K, Higaki K, Kimura T. Evaluation of in vivo dissolution behavior and GI transit of griseofulvin, a BCS class II drug. Int J Pharm. 2008;352[1-2]:36–43. doi: 10.1016/j.ijpharm.2007.10.008. [PubMed] [CrossRef] [Google Scholar]

6. Kreilgaard M. Influence of microemulsions on cutaneous drug delivery. Adv Drug Deliv Rev. 2002;54 Suppl 1:S77–98. [PubMed] [Google Scholar]

7. Radomska-Soukharev A, Wojciechowska J. Microemulsions as potential ocular drug delivery systems: phase diagrams and physical properties depending on ingredients. Acta Pol Pharm. 2005;62[6]:465–71. [PubMed] [Google Scholar]

8. Zvonar A, Rozman B, Rogac MB, Gasperlin M. The influence of microstructure on celecoxib release from a pharmaceutically applicable system: Mygliol 812/Labrasol /Plurol Oleique /Water mixtures. Acta Chim Slov. 2009;56[1]:131–8. [Google Scholar]

9. Trotta M, Gallarate M, Carlotti ME, Morel S. Preparation of griseofulvin nanoparticles from water-dilutable microemulsions. Int J Pharm. 2003;254[2]:235–42. doi: 10.1016/s0378-5173[03]00029-2. [PubMed] [CrossRef] [Google Scholar]

10. Nandi I, Bari M, Joshi H. Study of isopropyl myristate microemulsion systems containing cyclodextrins to improve the solubility of 2 model hydrophobic drugs. AAPS PharmSciTech. 2003;4[1]:E10. doi: 10.1208/pt040110. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

11. Bajpai M, Sharma PK, Mittal A. A Study of oleic acid oily base for the tropical delivery of dexamethasone microemulsion formulation. Asian J Pharm. 2009;3[3]:208–14. doi: 10.4103/0973-8398.56299. [CrossRef] [Google Scholar]

12. Paul BK, Moulik SP. Uses and applications of microemulsions. Curr Sci. 2001;80[8]:990–1001. [Google Scholar]

13. Moghimipour E, Salimi A, Karami M, Isazadeh S. Preparation and characterization of dexamethasone microemulsion based on pseudoternary phase diagram. Jundishapur J Nat Pharm Prod. 2013;8[3]:105–12. [PMC free article] [PubMed] [Google Scholar]

14. Hathout RM, Woodman TJ, Mansour S, Mortada ND, Geneidi AS, Guy RH. Microemulsion formulations for the transdermal delivery of testosterone. Eur J Pharm Sci. 2010;40[3]:188–96. doi: 10.1016/j.ejps.2010.03.008. [PubMed] [CrossRef] [Google Scholar]

15. Salimi A, Moghimipour E, Tavakolbekhoda N. Transdermal Delivery of CelecoxibThrough Rat Skin From Various Microemulsions. Int Res J Pharm Appl Sci. 2013;3[4]:173–81. [Google Scholar]

16. Chandra A, Sharma P, Irchhiaya R. Microemulsion-based hydrogel formulation for transdermal delivery of dexamethasone. Asian J Pharm. 2009;3[1]:30–6. doi: 10.4103/0973-8398.49172. [CrossRef] [Google Scholar]

17. Bagwe RP, Kanicky JR, Palla BJ, Patanjali PK, Shah DO. Improved drug delivery using microemulsions: Rationale, recent progress, and new horizons. Crit Rev Ther Drug Carrier Syst. 2001;18[1]:77–140. [PubMed] [Google Scholar]

18. Acharya A, Sanyal SK, Moulik SP. Formation and characterization of a pharmaceutically useful microemulsion derived from isopropylmyristate, polyoxyethylene [4] lauryl ether [Brij-30], isopropyl alcohol and water. Curr Sci. 2001;81[4]:362–70. [Google Scholar]

19. Raman IA, Suhaimi H, Tiddy GJ. Liquid crystals and microemulsions formed by mixtures of a non-ionic surfactant with palm oil and its derivatives. Adv Colloid Interface Sci. 2003;106:109–27. doi: 10.1016/S0001-8686[03]00107-6. [PubMed] [CrossRef] [Google Scholar]

20. Gradzielski M. Recent developments in the characterisation of microemulsions. Curr Opin Colloid Interface Sci. 2008;13[4]:263–9. doi: 10.1016/j.cocis.2007.10.006. [CrossRef] [Google Scholar]

21. Podlogar F, Gasperlin M, Tomsic M, Jamnik A, Rogac MB. Structural characterisation of water-tween 40/imwitor 308-isopropyl myristate microemulsions using different experimental methods. Int J Pharm. 2004;276[1-2]:115–28. doi: 10.1016/j.ijpharm.2004.02.018. [PubMed] [CrossRef] [Google Scholar]

22. Kumar P, Mittal KL. Handbook of Microemulsion Science and Technology. New York: Marcel Dekker; 1999. [Google Scholar]

23. Hirai M, Kawai-Hirai R, Sanada M, Iwase H, Mitsuya S. Characteristics of AOT Microemulsion Structure Depending on Apolar Solvents. J Phys Chem B. 1999;103[44]:9658–62. doi: 10.1021/jp991899d. [CrossRef] [Google Scholar]

24. Salimi A, Hedayatipour N, Moghimipour E. The Effect of Various Vehicles on the Naproxen Permeability through Rat Skin: A Mechanistic Study by DSC and FT-IR Techniques. Adv Pharm Bull. 2016;6[1]:9–16. doi: 10.15171/apb.2016.003. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

25. Leanpolchareanchai J, Padois K, Falson F, Bavovada R, Pithayanukul P. Microemulsion system for topical delivery of thai mango seed kernel extract: Development, physicochemical characterisation and ex vivo skin permeation studies. Molecules. 2014;19[11]:17107–29. doi: 10.3390/molecules191117107. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

26. Moghimipour E, Salimi A, Leis F. Preparation and evaluation of tretinoin microemulsion based on pseudo-ternary phase diagram. Adv Pharm Bull. 2012;2[2]:141–7. doi: 10.5681/apb.2012.022. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

27. Moghimipour E, Salimi A, Eftekhari S. Design and Characterization of Microemulsion Systems for Naproxen. Adv Pharm Bull. 2013;3[1]:63–71. doi: 10.5681/apb.2013.011. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

28. Salimi A, Sharif Makhmal Zadeh B, Moghimipour E. Preparation and Characterization of Cyanocobalamin [Vit B12] Microemulsion Properties and Structure for Topical and Transdermal Application. Iran J Basic Med Sci. 2013;16[7]:865–72. doi: 10.22038/ijbms.2013.1126. [PMC free article] [PubMed] [CrossRef] [Google Scholar]

29. Bumajdad A, Eastoe J. Conductivity of water-in-oil microemulsions stabilized by mixed surfactants. J Colloid Interface Sci. 2004;274[1]:268–76. doi: 10.1016/j.jcis.2003.12.050. [PubMed] [CrossRef] [Google Scholar]

30. Garti N, Aserin A, Tiunova I, Fanun M. A DSC study of water behavior in water-in-oil microemulsions stabilized by sucrose esters and butanol. Colloids Surf Physicochem Eng Aspects. 2000;170[1]:1–18. doi: 10.1016/S0927-7757[00]00486-6. [CrossRef] [Google Scholar]

31. Dong X, Ke X, Liao Z. The microstructure characterization of meloxicam microemulsion and its influence on the solubilization capacity. Drug Dev Ind Pharm. 2011;37[8]:894–900. doi: 10.3109/03639045.2010.548067. [PubMed] [CrossRef] [Google Scholar]

32. Zhang J, Michniak-Kohn B. Investigation of microemulsion microstructures and their relationship to transdermal permeation of model drugs: Ketoprofen, lidocaine, and caffeine. Int J Pharm. 2011;421[1]:34–44. doi: 10.1016/j.ijpharm.2011.09.014. [PubMed] [CrossRef] [Google Scholar]

33. Luzzati V, Mustacchi H, Skoulios A, Husson F. La structure des colloides d'association. I. Les phases liquide-cristallines des systemes amphiphile-eau. Acta Cryst. 1960;13:660–7. doi: 10.1107/S0365110X60001564. [CrossRef] [Google Scholar]

34. Mueller-Goymann CC. Liquid crystals in drug delivery. In: Swarbrick J, Boylan JC, editors. Encyclopedia of Pharmaceutical Technology. New York: Marcel Dekker Inc; 2002. P. 834-53.

35. Fontell K, Mandell L, Ekwall P. Some isotropic mesophases in systems containing amphiphilic compounds. Acta Chem Scand. 1968;22[10]:3209–23. doi: 10.3891/acta.chem.scand.22-3209. [CrossRef] [Google Scholar]

36. Bunjes H, Rades T. Thermotropic liquid crystalline drugs. J Pharm Pharmacol. 2005;57[7]:807–16. doi: 10.1211/0022357056208. [PubMed] [CrossRef] [Google Scholar]

37. Strey R. Microemulsion microstructure and interfacial curvature. Colloid Polym Sci. 1994;272[8]:1005–19. doi: 10.1007/BF00658900. [CrossRef] [Google Scholar]

38. Omray LK. Liquid Crystals as Novel Vesicular Delivery System: A Review. Curr Trends Technol Sci. 2013;2[6]:347–51. [Google Scholar]

39. Yaghmur A, Glatter O. Characterization and potential applications of nanostructured aqueous dispersions. Adv Colloid Interface Sci. 2009;147-148:333–42. doi: 10.1016/j.cis.2008.07.007. [PubMed] [CrossRef] [Google Scholar]

40. Sagalowicz L, Leser ME, Watzke HJ, Michel M. Monoglyceride self-assembly structures as delivery vehicles. Trends Food Sci Technol. 2006;17[5]:204–14. doi: 10.1016/j.tifs.2005.12.012. [CrossRef] [Google Scholar]

Page 2

The equilibrium Solubility of Griseofulvin in Various Oils, Surfactants and Cosurfactants [Mean ± SD, n = 3]

Phase type Excipient Solubility [mg/ml]
oilOleic acid2.66 ± 0.15
Oleic acid + transcutol P3.61 ± 0.04
Isopropyl Myristat2.01 ± 0.07
IsopropyMyristat + transcutol3.50 ± 0.20
surfactantTween 803.06 ± 0.30
Span 203.09 ± 0.10
Labrasol4.36 ± 0.15
co-surfactantPleurol Oleic2.60 ± 0.10
Propylene glycol1.00 ± 0.01

Video liên quan

Chủ Đề