alexa Pharmaceutical Nanocarriers (Liposomes and Micelles) in Cancer Therapy | Open Access Journals
ISSN: 2157-7439
Journal of Nanomedicine & Nanotechnology
Like us on:
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Pharmaceutical Nanocarriers (Liposomes and Micelles) in Cancer Therapy

Onkar S. Vaze*

100 Corporate Drive, South Plainfield, New Jersey, U.S.A., 07080

*Corresponding Author:
Vaze OS
100 Corporate Drive, South Plainfield
NJ 08863, USA
Tel: 1 9089129255
E-mail: [email protected]

Received date May 03, 2016; Accepted date May 05, 2016; Published date May 12, 2016

Citation: Vaze OS (2016) Pharmaceutical Nanocarriers (Liposomes and Micelles) in Cancer Therapy. J Nanomed Nanotechnol 7:e138. doi:10.4172/2157- 7439.1000e138

Copyright: © 2016 Vaze OS. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Journal of Nanomedicine & Nanotechnology


Editorial

Fundamental progress in cancer biology has resulted in remarkable advances in diagnosis and cancer therapy. The need now is to transform this knowledge into effective therapies. The effectiveness of chemotherapeutic drugs is severely limited due to the dose-limiting toxicity and patient morbidity. In cancer therapy, effective delivery of the drug to the tumor site while avoiding off-site side effects is the primary challenge. This challenge can be overcome by targeting the tumor site selectively to avoid the undesired side-effects at non-target sites after the systemic delivery. A good drug delivery system fulfills several pharmaceutical requirements including increase in therapeutic effect, good biocompatibility, an ability to accumulate at a targeted site and controlled release of the drug at the target site [1]. Nanocarriers assisted delivery of drugs has become a successful strategy that enhances the delivery of small molecule and large molecules such a genes and peptides or proteins [2]. Different nanocarriers such as nanospheres, nanocapsules, liposomes, micelles, dendrimers, quantum dots, solid lipid nanoparticles, polymeric nanoparticles, gold nanoparticles, virus and virus-like nanoparticles have been explored for the delivery of small molecules and large molecules therapeutics.

Liposomes and micelles are the most extensively studied and understood pharmaceutical nanocarriers. Cholesterol and phospholipid molecules, that normally form cell membranes, generate liposomes which are vesicular nanostructures. Therapeutic liposomes are 50-200 nm in size and can be loaded with water soluble therapeutic agents in the aqueous core and water insoluble therapeutic agents in phospholipid (hydrophobic) bilayer. Micelles are colloidal dispersion with a particle size between 5-100 nm. For pharmaceuticals with poor solubility, Micelles can improve the bioavailability and solubility. Therapeutic agents in conjunction with nanocarriers such as liposomes and micelles result in better pharmacokinetic properties of the carrier-loaded drugs thereby improving therapeutic activity. These systems provide easier control, composition, size and in vivo stability in comparison with other drug delivery systems [3]. Furthermore, preparation is considerably simpler and also small amounts of a targeting component can be attached to a these pharmaceutical nanocarriers. Thus, the fundamentals of liposomal and micellar nanocarrier and their biological interactions are well studied, and aids to design such nanocarriers with specific drug delivery, targeting and release characteristics. Lipid-or polymer-based delivery of therapeutic agent is the basic and simple nanotechnology platform which has found the most success in the clinics (Table 1).

Although an extensive number of scientific publications regarding these pharmaceutical nanocarriers exist, the translation of these pharmaceutical nanocarriers has been slow in comparison to that for small molecule drugs [4]. Lack of clear regulatory guidelines as well as technical issues are factors limiting the clinical application of nanomedicines [5].

As opposed to conventional drugs, the development of these technologies (nanomedicine/nanocarriers) combine expert knowledge from the fields of Chemistry, Biology and Physics. The products of these collaborations are wide ranging in concept and design. This conjunction of various academic disciplines in addition to a concerted effort by regulatory bodies and industry is required for advances in such technologies. With these stakeholders working in harmony, it is possible to steer future research to obtain nanomedicine products that are both effective and safe.

Pharmaceutical nanocarriers such as liposomes and micelles have the potential to create new sources of revenue for the pharmaceutical and biotech industries and will improve the life cycle of proprietary drugs [6]. It will revolutionize the field of medicine by creating new therapies. So far, academic departments, new startups and small technology companies seem to have invested more effort in such technologies [6- 14]. Drug delivery has already been revolutionized by nanotechnology. Pharmaceutical nanocarriers have made significant contributions to medicine and diagnostics and it will further continue to revolutionize these fields and further investigations are warranted in this area.

Pharmaceutical nanocarriers Trade/ProductName Drug Company Current Status Reference
Liposomes Onivyde Irinotecan Merrimack Pharmaceuticals Approved in October 2015 [14]
Maroqbio Vincristine sulfate Spectrum Pharamceuticals Approved in October 2012 [12]
Doxil Doxorubicin Janssen Biotech Approved in 1995 [7]
Mepact Mifamurtide Takeda Pharmaceuticals Phase III (USA)
Approved in Europe
[9]
ALN-VSP02 siRNA against VEGF and kinesin spindle protein Alnylam Pharmaceuticals Phase I [8]
Micelles Genexol-PM Paclitaxel Samyang Biopharma Approved (South Korea)
Phase II (USA)
[7]
  Paclical Paclitaxel Osamnia Pharamceutical Phase III [13]
  NC 6004 Cisplatin Nanocarrier Phase II [10]
  NK012 SN-38 Nippon Kayaku Co. Ltd Phase II [11]
  SP1049C Doxorubicin Supratek Pharmaceuticals Phase II [7]

Table 1: Selected list nanomedicines in oncology.

References

Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Recommended Conferences

  • Nano Congress for Next Generation
    August 31-September 01, 2017 Brussels,Belgium
  • Graphene & 2D Materials
    September 14-15, 2017 Edinburgh, Scotland
  • Graphene & 2D Materials
    November 6-7, 2017 Frankfurt, Germany
  • World Congress on Nanoscience and Nano Technology
    October 16-17, 2017 Dubai, UAE
  • World Medical Nanotechnology Congress
    October 18-19, 2017 Osaka, Japan
  • Nanoscienceand Molecular Nanotechnology
    Nov 06-08, 2017 Frankfurt, Germany

Article Usage

  • Total views: 8501
  • [From(publication date):
    June-2016 - Aug 22, 2017]
  • Breakdown by view type
  • HTML page views : 8376
  • PDF downloads :125
 

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

 
© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version
adwords