Active packaging for topical cosmetic/drug products: A hot-melt extruded preservative delivery device

European Journal of Pharmaceutics and Biopharmaceutics

Volumn 75, Issue 2, 2010, Pages 291-296

  Zema, L ^a   Sangalli, M E ^a   Maroni, A ^a   Foppoli, A ^a   Bettero, A ^b   Gazzaniga, A ^a  

^a UNIVERSITY OF MILAN   (Italy)

^b UNIVERSITY OF PADOVA   (Italy)

Author keywords

Active packaging; Hot melt extrusion; Inert matrices for prolonged release; Preservative; Simulation program

Indexed keywords

COSMETIC; DEHYDROACETIC ACID; POLYETHYLENE;

AQUEOUS SOLUTION; ARTICLE; COMPARTMENT MODEL; DEGRADATION KINETICS; DRUG DELIVERY SYSTEM; DRUG DESIGN; DRUG FORMULATION; DRUG RELEASE; MATRIX TABLET; PACKAGING MATERIAL; PELLET EXTRUSION; SCANNING ELECTRON MICROSCOPY;

ADMINISTRATION, CUTANEOUS; COMPUTER SIMULATION; COSMETICS; DELAYED-ACTION PREPARATIONS; DRUG DELIVERY SYSTEMS; DRUG PACKAGING; DRUG STABILITY; FORMALDEHYDE; HOT TEMPERATURE; POLYETHYLENE; PRESERVATIVES, PHARMACEUTICAL; PYRONES; TIME FACTORS;

EID: 77952959174     PISSN: 09396411     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejpb.2010.03.007     Document Type: Article

References (27)

1. Sasseville D. Hypersensitivity to preservatives. Dermatol. Ther. 2004, 17:251-263.
2. Rooney M.L. Active Food Packaging 1995, Blackie Academic & Professional, London.
3. Vermeiren L., Devlieghere F., Van Beest M., De Kruijf N., Debevere J. Developments in the active packaging of foods. Trends Food Sci. Technol. 1999, 10:77-86.
4. Ahvenainen R. Novel Food Packaging Techniques 2003, CRC Press, Boca Raton, FL.
5. Appendini P., Hotchkiss J.H. Review of antimicrobial food packaging. Innov. Food Sci. Emerg. Technol. 2002, 3:113-126.
6. Cutter C.N. Microbial control by packaging: a review. Crit. Rev. Food Sci. Nutrit. 2002, 42:151-161.
7. Suppakul P., Miltz J., Sonneveld K., Bigger S.W. Active packaging technologies with an emphasis on antimicrobial packaging and its applications. J. Food Sci. 2003, 68:408-420.
8. LaCoste A., Schaich K.M., Zumbrunnen D., Yam K.L. Advancing controlled release packaging through smart blending. Packaging Technol. Sci. 2005, 18:77-87.
9. Joerger R.D. Antimicrobial films for food applications: a quantitative analysis of their effectiveness. Packaging Technol. Sci. 2007, 20:231-273.
10. Schaich K.M., Obinata N., Yam K. Delivering natural antioxidants via controlled release packaging. Acta Hort. (ISHS) 2008, 778:53-64.
11. Chi-Zhang Y., Yam K.L., Chikindas M.L. Effective control of Listeria Monocytogenes by combination of nisin formulated and slowly released into a broth system. Int. J. Food Microbiol. 2004, 90:15-22.
12. J Kabara J. Cosmetic and Drug Preservation 1984, CRC Press, Boca Raton, FL.
13. Benassi C.A., Semenzato A., Lucchiari M., Bettero A. Dehydroacetic acid sodium salt stability in cosmetic preservative mixtures. Int. J. Cosmet. Sci. 1988, 10:29-37.
14. P.J. Lutz, A.M. Tafesh, Stable, low free formaldehyde, synergistic antimicrobial compositions of aldehyde donors and dehydroacetic acid, PCT Int. Appl. WO 2004/017736 A1.
15. Gazzaniga A., Sangalli M.E., Giordano F., Conte U., Semenzato A., Bettero A. Controlled release of dehydroacetic acid sodium salt for the stability improvement of cosmetic formulations. Int. J. Cosmet. Sci. 1994, 16:105-112.
16. M.E. Sangalli, A. Maroni, L. Zema, A. Foppoli, M. Cerea, F. Giordano, A. Gazzaniga, Compartment model-based simulation approach to the design of a matrix cosmetic preservative system. In: Proceed. 30th Int. Symp. Control. Rel. Bioact. Mater., Glasgow, UK, July 19-23, 2003.
17. Peppas N.A. Analysis of Fickian and non-Fickian drug release from polymers. Pharm. Acta Helv. 1985, 60:110-111.
18. Ramsay M.W., Grass G.M., Vallner J.J. Pharmacokinetic simulations using STELLA®: prediction of in vivo performance of oral dosage forms. Eur. J. Pharm. Biopharm. 1991, 37:192-197.
19. Grass G.M., Bozarth C.A., Vallner J.J. Evaluation of the performance of controlled-release dosage forms of ticlopidine using in vitro intestinal permeability and computer simulations. J. Drug Target. 1994, 2:23-33.
20. Grass G.M. Simulation models to predict oral drug absorption from in vitro data. Adv. Drug Deliv. Rev. 1997, 23:199-219.
21. Ranta V.P., Laavola M., Toropainen E., Vellonen K.S., Talvitie A., Urtti A. Ocular pharmacokinetic modeling using corneal absorption and desorption rates from in vitro permeation experiments with cultured corneal epithelial cells. Pharm. Res. 2003, 20:1409-1416.
22. Colombo P., Gazzaniga A., Caramella C., Conte U., La Manna A. In vitro programmable zero-order release drug delivery system. Acta Pharm. Technol. 1987, 33:15-20.
23. Grassi M., Zema L., Sangalli M.E., Maroni A., Giordano F., Gazzaniga A. Modeling of drug release from partially coated matrices made of a high viscosity HPMC. Int. J. Pharm. 2004, 276:107-114.
24. Béchard S., McMullen J.N. Solute release from a porous polymeric matrix: inwardly tapered disk with a central releasing hole. J. Pharm. Sci. 1988, 77:222-228.
25. Sangalli M.E., Giunchedi P., Maggi L., Conte U., Gazzaniga A. Inert monolithic device with a central hole for constant drug release. Eur. J. Pharm. Biopharm. 1994, 40:370-373.
26. Sangalli M.E., Maroni A., Zema L., Cerea M., Conte U., Gazzaniga A. A study on the release mechanism of drugs from hydrophilic partially coated perforated matrices. Farmaco 2003, 58:971-976.
27. Colombo P., Bettini R., Catellani P., Santi P., Peppas N.A. Drug volume fraction profile in the gel phase and drug release kinetics in hydroxypropyl methylcellulose matrices containing a soluble drug. Eur. J. Pharm. Sci. 1999, 9:33-40.