Skin permeation of cacalol, cacaloneand 6-epi-cacalone sesquiterpenes from a nanoemulsion

Natural Product Communications

Volumn 7, Issue 7, 2012, Pages 821-823

  Garduño Ramírez, María Luisa ^a   Clares, Beatriz ^b   Domínguez Villegas, Valeri ^c   Peraire, Concepción ^c   Ruiz, María Adolfina ^b   García, María Luisa ^c   Calpena, Ana C ^c  

^a CENTRO DE INVESTIGACIONES QUÍMICAS   (Mexico)

^b UNIVERSITY OF GRANADA   (Spain)

^c UNIVERSITY OF BARCELONA   (Spain)

Author keywords

Cacalol; Cacalone; Diclofenac acid; Nanoemulsion; Permeation

Indexed keywords

6 EPI CACALOLONE; CACALOL; CACALOLONE; DICLOFENAC; FATTY ACID; GLYCEROL DIOLEATE; LABRASOL; MEDIUM CHAIN TRIACYLGLYCEROL; PLANT EXTRACT; PROPYLENE GLYCOL; PSACALIUM RADULIFOLIUM EXTRACT; SESQUITERPENE; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; DRUG FORMULATION; DRUG PENETRATION; DRUG STRUCTURE; HUMAN; HUMAN EXPERIMENT; MEDICINAL PLANT; NANOEMULSION; NORMAL HUMAN; PLANT ROOT; PSACALIUM RADULIFOLIUM; QUANTITATIVE ANALYSIS; SKIN PENETRATION; VOLUNTEER;

ADMINISTRATION, CUTANEOUS; ANIMALS; EMULSIONS; HUMANS; SESQUITERPENES; SKIN ABSORPTION;

EID: 84864642707     PISSN: 1934578X     EISSN: 15559475     Source Type: Journal    
DOI: None     Document Type: Article

References (14)

1. Garduño-Ramírez ML, Trejo A, Navarro V, Bye R, Linares E, Delgado G. (2001) New modified eremophilanes from the roots of Psacalium radulifolium. Journal of Natural Products, 64, 432-435.
2. Garduño-Ramírez ML, Delgado G. (2003) New eremophilanoids from the roots of Psacalium radulifolium. Hypoglycemic, antihyperglycemic and anti-oxidant evaluations. Revista de la Sociedad Química de México, 47, 155-159.
3. Acevedo-Quiroz N, Domínguez-Villegas V, Garduño- Ramírez ML. (2008) Structure-activity relationship of modified eremophilanes and antiinflammatory activity using the TPA mouse edema ear test. Natural Product Communications, 3, 313-317.
4. Escribano E, Calpena AC, Queralt J, Obach R, Domenech J. (2003) Assessment of diclofenac permeation with different formulations: antiinflammatory study of a selected formula. European Journal of Pharmaceutical Science, 19, 203-210. (Pubitemid 36918412)
5. Sintov AC, Botner S. (2006) Transdermal drug delivery using microemulsion and aqueous systems: Influence of the skin storage conditions on the in vitro permeability of diclofenac from aqueous vehicle systems. International Journal of Pharmaceutics, 311, 55-62.
6. Clares B, Gallardo V, Medina MM, Ruíz MA. (2009) Multilamellar liposomes of triamcinolone acetonide: preparation, stability and characterization. Journal of Liposome Research, 19, 197-206.
7. Ruiz MA, Clares B, Morales ME, Gallardo V. (2008) Vesicular lipidic systems, liposomes, PLO, and liposomes-PLO: characterization by electronic transmission microscopy. Drug Development and Industrial Pharmacy, 34, 1269-1276.
8. Shafiq S, Faiyaz S, Sushma T, Farhan JA, Khar RK, Ali M. (2007) Design and development of ramipril nanoemulsion formulation: In vitro and in vivo assessment. Journal of Biomedical Nanotechnology, 3, 28-44. (Pubitemid 351877125)
9. Shafiq S, Faiyaz S, Sushma T, Farhan JA, Khar RK, Ali M. (2007) Development and bioavailability assessment of ramipril nanoemulsion formulation. European Journal of Pharmaceutics and Biopharmaceutics, 66, 227-243. (Pubitemid 46667230)
10. Abisma B, Canselier JP, Wilhelm AM, Delmas H, Gourdon C. (1999) Emulsification by ultrasound: drop size distribution and stability. Ultrasonics Sonochemistry, 6, 75-83.
11. Gattefossé SA. (1994) Microemulsion: Formulation Guide, Publication No. PF9225A, Saint-Priest Cedex, France.
12. Levitt M, Perutz MF. (1988) Aromatic rings act as hydrogen bond acceptors. Journal of Molecular Biology, 201, 751-754.
13. Tadros, T, Izquierdo, P, Esquena J, Solans C. (2004) Formation and stability of nano-emulsions. Advances in Colloid and Interface Science, 108, 303-318.
14. Cevc G. (2004) Lipid vesicles and others colloids as drug carriers on the skin. Advanced Drug Delivery Reviews, 56, 675-711.