Microsponges as Innovative Drug Delivery Systems

DOI:

https://doi.org/10.37285/ijpsn.2012.5.1.2

Authors

  • Dipit Jagannath Ingale
  • N H Aloorkar
  • A S KulkarnI
  • R.A. Patil Patil

Abstract

Transdermal drug delivery system (TDDS) is not practicable for delivery of materials whose final target is skin itself. Controlled release of drugs onto the epidermis with assurance that the drug remains primarily localized and does not enter the systemic circulation in significant amounts is a challenging area of research. Microsponges are highly porous micro-sized particles with a unique ability for entrapping active pharmaceutical ingredients. To control the delivery rate of active agents to a predetermined site in human body has been one of the biggest challenges faced by scientists. Microsponges are safe biologically and offer unique advantage of programmable release. This technology offers entrapment of ingredients and is believed to contribute towards reduced side effects, improved stability, increased elegance and enhanced formulation flexibility. This technology is being used for topical formulations and also for oral administration. The present review describes microsponge technology including its preparation, characterization, programmable parameters and release mechanism of microsponge drug delivery system.

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Keywords:

Microsponges, transdermal drug delivery, programmable release, topical formulation, oral administration

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Published

2012-05-31

How to Cite

1.
Ingale DJ, Aloorkar NH, KulkarnI AS, Patil RP. Microsponges as Innovative Drug Delivery Systems. Scopus Indexed [Internet]. 2012 May 31 [cited 2024 Dec. 22];5(1):1597-606. Available from: https://ijpsnonline.com/index.php/ijpsn/article/view/560

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Section

Review Articles

References

Anderson D.L., Cheng C.H., Nacht S (1994). Flow Characteristics of Loosely Compacted Macroporous Microsponge(R) Polymeric Systems. Powder Technol 78: 15-18.

Aritomi H., Yamasaki Y., Yamada K., Honda H., Koshi M (1996). Development of sustained release formulation of chlorpheniramine maleate using powder coated microsponges prepared by dry impact blending method. J Pharm Sci Technol 56(1):49-56.

Barkai A., Pathak V., Benita S (1990). Polyacrylate (Eudragit retard) microspheres for oral controlled release of nifedipine. I. Formulation design and process optimization. Drug Dev Ind Pharm 16: 2057-2075.

Cavalli R, Tumiatii WJ (2006). Inclusion Phenomena and Macrocyclic Chemistry 56: 209-213.

Chadawar V., Shaji J (2007). Microsponge delivery. Curr Drug Deliv 4:123–129.

Chowdary K.P.R., and Rao Y.S (2004). Mucoadhesive Micro-spheres for Controlled Drug Delivery, Biol Pharm Bull 11: 1717-1724.

Christensen M.S. and Natch S.J. Invest. Dermato. 1983; 69:282.

D’souza J.I., More H.N (2008). Topical Anti-Inflammatory Gels of Fluocinolone Acetonide Entrapped in Eudragit Based Microsponge Delivery System. Res J Pharm Tech 1(4):502-506.

D’souza JI (2008). The Microsponge Drug Delivery System: For Delivering an Active Ingredient by Controlled Time Release. Pharma. info.net 6(3): 62.

D'souza JI (2001). In vitro Antibacterial and Skin Irritation Studies of Microsponges of Benzoyl Peroxide. Ind Drugs 38(7): 104-109.

D'souza J.I., Saboji J.K., Suresh G (2004). Design and evaluation of benzoyl peroxide microsponges to enhance therapeutic efficacy in acne treatment. Accepted for presentation in 20th FAPA Congress, Bangkok, Thailand 2:26.

Emanuele A.D. and Dinarvand R (1995). Preparation, characterization and drug release from thermo responsive microspheres. Int. J. Pharm 118:237-242.

Embil K. and Nacht S.J (1996). The microsponge delivery system (MDS): a topical delivery system with reduced irritancy incorporating multiple triggering mechanisms for the release of actives. J. Microencapsul 13(5):575-588.

Franz T.J (1975). Percutaneous absorption. On the relevance of in vitro date. J Invest Dermatol 22:499 – 505.

Jelvehgari M., Siahi-Shadbad M.R., Azarmi S., Gary P., Martin A., Nokhodchi A (2006). The microsponge delivery system of benzoyl peroxide: Preparation, characterization and release studies. Int J Pharm 308:124-132.

Kawashima Y., Niwa T., Takeuchi H., Hino T. and Itoh Y (1991). Control of prolonged drug release and compression properties of Ibuprofen microsponges with acrylic polymer, eudragit RS, by changing their intraparticle density. Chem Pharm Bull 19:279-290.

Kawashima Y., Niwa T., Takeuchi H., Hino T. and Itoh Y (1991). Furuyama S.characterization of polymorphs of tranilast anhydrate and tranilast monohydrate when crystallized by two solvent change spherical crystallization techniques. J Pharm Sci 80: 472-478.

Khopade AJ, Jain S, Jain NK (1996). The Microsponge. Eastern Pharmacist :49-53.

Kilicarslan, Baykara T (2003). The effect of the drug/polymer ratio on the properties of verapamil HCl loaded microspheres. Int J Pharm 252:99-109.

Kydonieus A.F. and Berner B (1987). Transdermal delivery of drugs, CRC Press, Boca Raton.

Martin A., Swarbrick J. and Cammarrata A (1991), In: Physical Pharmacy- Physical Chemical Principles in Pharmaceutical Sciences 3:527.

Mine O., Erdal C., Ahmet A (2006). Design and evaluation of colon specific drug delivery system containing flurbiprofen microsponges. Int J Pharm 318:103-117.

Orr Jr., C (1969). Application of mercury penetration to material analysis. Powder Technol 3: 117–123.

Poresizer Model No. 9310, Micromeritics Instrument Corp., Nor-cross , Georgia.

Shah VP (2007). Determination of In-vitro Release from Hydrocortisone Creams. International Journal of Pharmaceutics. 1989; 53: 53-59.

Swaminathan S., Torne S.J. Inclusion phenomena and Macrocyclic Chemistry 57: 89-94.

Tansel C., Omoglu C.T., Baykara T (2002). The effects of pressure and direct compression on tabletting of microsponges. Int J Pharm 242: 191-195.

Tansel C., Omoglu. T.B (2003). Preparation and in vitro evaluation of modified release ketoprofen Microsponges, II Farmaco 58: 101-106.

Vyas S.P., Khar R.K (2002). Targeted and Controlled Drug Delivery-Novel Carrier System: New Delhi: CBS Publication, First edition; 453.

Washburn EW (1971). Note on a method of determining the distribution of pore sizes in a porous material. Proc Natl Acad Sci U S A 7(4):115-116.

Won R (1992). United States Patent 5145675. Two step method for preparation of controlled release formulations.

Won R (1987). United States Patent 4690825. Method for delivering an active ingredient by controlled time release utilizing a novel delivery vehicle which can be prepared by a process utilizing active ingredient as a porogen.