全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Lipid Based Vesicular Drug Delivery Systems

DOI: 10.1155/2014/574673

Full-Text   Cite this paper   Add to My Lib

Abstract:

Vesicular drug delivery system can be defined as highly ordered assemblies consisting of one or more concentric bilayers formed as a result of self-assembling of amphiphilic building blocks in presence of water. Vesicular drug delivery systems are particularly important for targeted delivery of drugs because of their ability to localize the activity of drug at the site or organ of action thereby lowering its concentration at the other sites in body. Vesicular drug delivery system sustains drug action at a predetermined rate, relatively constant (zero order kinetics), efficient drug level in the body, and simultaneously minimizes the undesirable side effects. It can also localize drug action in the diseased tissue or organ by targeted drug delivery using carriers or chemical derivatization. Different types of pharmaceutical carriers such as polymeric micelles, particulate systems, and macro- and micromolecules are presented in the form of novel drug delivery system for targeted delivery of drugs. Particulate type carrier also known as colloidal carrier system, includes lipid particles, micro- and nanoparticles, micro- and nanospheres, polymeric micelles and vesicular systems like liposomes, sphingosomes, niosomes, transfersomes, aquasomes, ufasomes, and so forth. 1. Introduction In the past few decades, considerable attention has been paid to the development of novel drug delivery system. The novel drug delivery systems aim to fulfill two prerequisites; that is, it delivers the drug at a rate directed by the needs of the body, over the period of treatment, and it carries the drug directly to the inflamed tissues and/or organ. Conventional delivery systems including prolonged release dosage forms are unable to meet none of these. Novel drug delivery system sustains drug action at a predetermined rate, relatively constant (zero order kinetics), efficient drug level in the body, and simultaneously minimizes the undesirable side effects. It can also localize drug action in the diseased tissue or organ by targeted drug delivery using carriers or chemical derivatization. Different types of pharmaceutical carriers such as polymeric micelles, particulate systems, and macro- and micromolecules are presented in the form of novel drug delivery system for targeted delivery of drugs. Particulate type carrier, also known as colloidal carrier system, includes lipid particles, micro- and nanoparticles, micro- and nanospheres, polymeric micelles, and vesicular systems like liposomes, sphingosomes, niosomes, transfersomes, aquasomes, ufasomes, and so forth. 1.1. Lipid

References

[1]  K. Sashi, K. Satinder, and P. Bharat, “A complete review on: liposomes,” International Research Journal of Pharmacy, vol. 3, no. 7, pp. 10–16, 2012.
[2]  S. M. Jadhav, P. Morey, M. M. Karpe, and V. Kadam, “Novel vesicular system: an overview,” Journal of Applied Pharmaceutical Science, vol. 2, no. 1, pp. 193–202, 2012.
[3]  R. Z. Mujoriya, K. Dhamande, and R. B. Bodla, “Niosomal drug delivery system—a review,” International Journal of Applied Pharmaceutics, vol. 3, no. 3, pp. 7–10, 2011.
[4]  K. Abhinav, P. J. Lal, J. Amit, and S. Vishwabhan, “Review on niosomes as novel drug delivery system,” International Research Journal of Pharmacy, vol. 2, no. 5, pp. 61–65, 2011.
[5]  S. T. Prajapati, C. G. Patel, and C. N. Patel, “Transfersomes: a vesicular carrier system for transdermal drug delivery,” Asian Journal of Biochemical and Pharmaceutical Research, vol. 2, no. 1, pp. 507–524, 2011.
[6]  S. M. Gavali, S. S. Pacharane, K. R. Jadhav, and V. J. Kadam, “Clinical transfersome: a new technique for transdermal drug delivery,” International Research Journal of Pharmacy and Chemistry, vol. 1, no. 3, pp. 735–740, 2011.
[7]  S. S. Jain, P. S. Jagtap, N. M. Dand, K. R. Jadhav, and V. J. Kadam, “Aquasomes: a novel drug carrier,” Journal of Applied Pharmaceutical Science, vol. 2, no. 1, pp. 184–192, 2012.
[8]  J. K. Patel, K. N. Patel, H. K. Patel, B. A. Patel, and P. A. Patel, “Aquasomes: a self assembling nanobiopharmaceutical carrier system for bio-active molecules: a review,” International Journal for Pharmaceutical Research Scholars, vol. 1, no. 1, pp. 11–21, 2012.
[9]  D. Lee and D. A. Weitz, “Double emulsion-templated nanoparticle colloidosomes with selective permeability,” Advanced Materials, vol. 20, no. 18, pp. 3498–3503, 2008.
[10]  S. Saraf, R. Rathi, C. D. Kaur, and S. Saraf, “Colloidosomes an advanced vesicular system in drug delivery,” Asian Journal of Scientific Research, vol. 4, no. 1, pp. 1–15, 2011.
[11]  R. R. Bhosale, R. A. Osmani, B. R. Harkare, and P. P. Ghodake, “Cubosomes: the inimitable nanoparticulate drug carriers,” Scholars Academic Journal of Pharmacy, vol. 2, no. 6, pp. 481–486, 2013.
[12]  D. Prashar and S. Dharmesh, “Cubosomes: a sustained drug delivery carrier,” Asian Journal of Research in Pharmaceutical Sciences, vol. 1, no. 3, pp. 59–62, 2011.
[13]  S. Lankalapalli and M. Damuluri, “Sphingosomes: applications in targeted drug delivery,” International Journal of Pharmaceutical,Chemical and Biological Sciences, vol. 2, no. 4, pp. 507–516, 2012.
[14]  K. Ashok, A. Rajendra Kumar, S. Nama, B. Brahmaiah, P. K. Desu, and C. B. Rao, “Sphingosomes: a novel vesicular drug delivery system,” International Journal of Pharmaceutical Research and Bio-Science, vol. 2, no. 2, pp. 305–312, 2013.
[15]  S. Saraf, D. Gupta, C. D. Kaur, and S. Saraf, “Sphingosomes a novel approach to vesicular drug delivery,” International Journal of Current Scientific Research, vol. 1, no. 2, pp. 63–68, 2011.
[16]  M. Rajkamal, S. Arwind, and A. Sandeep, “Exploring potential of ufasomes as topical/transdermal delivery systems: reviewing decades of research,” American Journal of Pharma Tech Research, vol. 2, no. 1, p. 12, 2012.
[17]  E. Moghimipour, M. Tafaghodi, A. Balouchi, and S. Handali, “Formulation and in vitro evaluation of topical liposomal gel of Triamcinolone acetonide,” Research Journal of Pharmaceutical, Biological and Chemical Sciences, vol. 4, no. 1, pp. 101–107, 2013.
[18]  P. Divakar, D. Kumar, C. Praveen, C. Sowmya, and C. Suryaprakash Reddy, “Formulation and in vitro evaluation of liposomes containing metformin hydrochloride,” International Journal of Research in Pharmaceutical and Biomedical Sciences, vol. 4, no. 2, pp. 479–485, 2013.
[19]  U. D. Shivhare, P. B. Suruse, and V. S. Thombare, “Formulation and in vitro evaluation of salbutamol sulfate liposomes,” American Journal of Pharmtech Research, vol. 2, no. 4, pp. 970–981, 2012.
[20]  N. Manjunatha, G. P. Naidu, V. Sutrave, K. Patel, and M. K. Samanta, “Preparation and evaluation of liposomes of an antiviral drug,” Indian Journal of Novel Drug Delivery, vol. 1, no. 1, pp. 25–31, 2009.
[21]  U. D. Shivhare, D. U. Ambulkar, V. B. Mathur, K. P. Bhusari, and M. D. Godbole, “Formulation and evaluation of pentoxifylline liposome formulation,” Digest Journal of Nanomaterials and Biostructures, vol. 4, no. 4, pp. 857–862, 2009.
[22]  R. P. Patel, H. Patel, and A. H. Baria, “Formulation and evaluation of liposomes of ketoconazole,” International Journal of Drug Delivery Technology, vol. 1, no. 1, pp. 16–23, 2009.
[23]  R. Agarwal, O. P. Katare, and S. P. Vyas, “Preparation and in vitro evaluation of liposomal/niosomal delivery systems for antipsoriatic drug dithranol,” International Journal of Pharmaceutics, vol. 228, no. 1-2, pp. 43–52, 2001.
[24]  P. Srinath, S. P. Vyas, and P. V. Diwan, “Preparation and pharmacodynamic evaluation of liposomes of indomethacin,” Drug Development and Industrial Pharmacy, vol. 26, no. 3, pp. 313–321, 2000.
[25]  M. Glavas-Dodov, E. Fredro-Kumbaradzi, K. Goracinova, S. Calis, M. Simonoska, and A. A. Hincal, “5-Fluorouracil in topical liposome gels for anticancer treatment—formulation and evaluation,” Acta Pharmaceutica, vol. 53, no. 4, pp. 241–250, 2003.
[26]  V. Dubey, D. Mishra, and N. K. Jain, “Melatonin loaded ethanolic liposomes: Physicochemical characterization and enhanced transdermal delivery,” European Journal of Pharmaceutics and Biopharmaceutics, vol. 67, no. 2, pp. 398–405, 2007.
[27]  R. Parthibarajan, S. Pradeep Kumar, N. L. Gowri Shankar et al., “Design and evaluation of voriconazole niosomes,” International Journal of Pharmacy and Pharmaceutical Sciences, vol. 5, no. 3, pp. 604–611, 2013.
[28]  A. N. Allam, S. S. E. Gamal, and V. F. Naggar, “Formulation and evaluation of Acyclovir niosomes for ophthalmic use,” Asian Journal of Pharmaceutical and Biological Research, vol. 1, no. 1, pp. 28–40, 2011.
[29]  V. Sathyavathi, A. Abdul Hasanthali, R. Ilaavrasan, and T. Sangeetha, “Formulation and evaluation of niosomal in situ gel ocular delivery system of brimonidine tartrate,” International Journal of Life Science and Pharma Research, vol. 2, no. 1, pp. L-82–L-95, 2012.
[30]  N. P. Rani, T. N. K. Suriyaprakash, and R. Senthamarai, “Formulation and evaluation of rifampicin and gatifloxacin niosomes on logarithmic-phase cultures of Mycobacterium tuberculosis,” International Journal of Pharma and Bio Sciences, vol. 1, no. 4, pp. 379–387, 2010.
[31]  M. Ning, Y. Guo, H. Pan, X. Chen, and Z. Gu, “Preparation, in vitro and in vivo evaluation of liposomal/niosomal gel delivery systems for clotrimazole,” Drug Development and Industrial Pharmacy, vol. 31, no. 4-5, pp. 375–383, 2005.
[32]  S. Mura, F. Pirot, M. Manconi, F. Falson, and A. M. Fadda, “Liposomes and niosomes as potential cariers for dermal delivery of minoxidil,” Journal of Drug Targeting, vol. 15, no. 2, pp. 101–108, 2007.
[33]  A. S. Guinedi, N. D. Mortada, S. Mansour, and R. M. Hathout, “Preparation and evaluation of reverse-phase evaporation and multilamellar niosomes as ophthalmic carriers of acetazolamide,” International Journal of Pharmaceutics, vol. 306, no. 1-2, pp. 71–82, 2005.
[34]  K. Ruckmani, B. Jayakar, and S. K. Ghosal, “Nonionic surfactant vesicles (niosomes) of cytarabine hydrochloride for effective treatment of leukemias: encapsulation, storage, and in vitro release,” Drug Development and Industrial Pharmacy, vol. 26, no. 2, pp. 217–222, 2000.
[35]  S. Duangjit, P. Opanasopit, T. Rojanarata, and T. Ngawhirunpat, “Evaluation of meloxicam-loaded cationic transfersomes as transdermal drug delivery carriers,” AAPS PharmSciTech, vol. 14, no. 1, pp. 133–140, 2013.
[36]  M. Irfan, S. Verma, and A. Ram, “Preparation and characterization of Ibuprofen loaded transferosome as a novel carrier for transdermal drug delivery system,” Asian Journal of Pharmaceutical and Clinical Research, vol. 5, no. 3, pp. 162–165, 2012.
[37]  S. Duangjit, P. Opanasopit, T. Rojanarata, and T. Ngawhirunpat, “Characterization and in vitro skin permeation of meloxicam-loaded liposomes versus transfersomes,” Journal of Drug Delivery, vol. 2011, Article ID 418316, 9 pages, 2011.
[38]  R. Patel, S. K. Singh, S. Singh, N. R. Sheth, and R. Gendle, “Development and characterization of curcumin loaded transfersome for transdermal delivery,” Journal of Pharmaceutical Sciences and Research, vol. 1, no. 4, pp. 71–80, 2009.
[39]  S. Jain, P. Jain, R. B. Umamaheshwari, and N. K. Jain, “Transfersomes—a novel vesicular carrier for enhanced transdermal delivery: development, characterization, and performance evaluation,” Drug Development and Industrial Pharmacy, vol. 29, no. 9, pp. 1013–1026, 2003.
[40]  B. K. Nanjwade, G. M. Hiremath, F. V. Manvi, and T. Srichana, “Formulation and evaluation of etoposide loaded aquasomes,” Journal of Nanopharmaceutics and Drug Delivery, vol. 1, pp. 92–101, 2013.
[41]  P. Vengala, S. Aslam, and C. V. S. Subhramanyam, “Development and in vitro evaluation of ceramic nanoparticles of piroxicam,” Latin American Journal of Pharmacy, vol. 32, no. 8, pp. 1124–1130, 2013.
[42]  T. Tiwari, S. Khan, N. Rao, A. Josh, and B. K. Dubey, “Preparation and characterization of aquasome based formulation of dianthrol for the treatment of psoriasis,” World Journal of Pharmacy and Pharmaceutical Sciences, vol. 1, no. 1, pp. 250–272, 2012.
[43]  S. Kommineni, S. Ahmad, P. Vengala, and C. V. S. Subramanyam, “Sugar coated ceramic nanocarriers for the oral delivery of hydrophobic drugs: formulation, optimization and evaluation,” Drug Development and Industrial Pharmacy, vol. 38, no. 5, pp. 577–586, 2012.
[44]  A. K. Cherian, A. C. Rana, and S. K. Jain, “Self-assembled carbohydrate-stabilized ceramic nanoparticles for the parenteral delivery of insulin,” Drug Development and Industrial Pharmacy, vol. 26, no. 4, pp. 459–463, 2000.
[45]  Y. R. Hundekar, J. K. Saboji, S. M. Patil, and B. K. Nanjwade, “Preparation and evaluation of diclofenac sodium cubosomes for percutaneous administration,” World Journal of Pharmacy and Pharmaceutical Sciences, vol. 3, no. 1, pp. 523–539, 2014.
[46]  Z. Yang, Y. Tan, M. Chen et al., “Development of amphotericin B-loaded cubosomes through the SolEmuls technology for enhancing the oral bioavailability,” AAPS PharmSciTech, vol. 13, no. 4, pp. 1483–1491, 2012.
[47]  C. Wu, Z. Yang, X. Peng et al., “Optimization of the preparation process for an oral phytantriol-based amphotericin B cubosomes,” Journal of Nanomaterials, vol. 2011, Article ID 308016, 10 pages, 2011.
[48]  S. Han, J.-Q. Shen, Y. Gan et al., “Novel vehicle based on cubosomes for ophthalmic delivery of flurbiprofen with low irritancy and high bioavailability,” Acta Pharmacologica Sinica, vol. 31, no. 8, pp. 990–998, 2010.
[49]  N. M. Morsi, G. A. Abdelbary, and M. A. Ahmed, “Silver sulfadiazine based cubosome hydrogels for topical treatment of burns: Development and in vitro/in vivo characterization,” European Journal of Pharmaceutics and Biopharmaceutics, vol. 86, no. 2, pp. 178–189, 2013.
[50]  Y. S. Tu, J. W. Fu, D. M. Sun et al., “Preparation, characterisation and evaluation of curcumin with piperine-loaded cubosome nanoparticles,” Journal of Microencapsulation, vol. 31, no. 6, pp. 551–559, 2014.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133