Abstract
Background: We have designed and patented a novel nanocarrier system to specifically deliver IL-2 to tumor cells expressing the IL-2 receptor (IL-2R). In this work, we provide data of the physical characteristics of the system, such as size, complexity and viscosity, stability to light, pH and temperature, pharmacodynamic and pharmacokinetic parameters, as well as toxic and antitumor properties. The nanocarrier system consists of positively charged liposomes that present non-covalently bound IL-2 molecules on their external surface to facilitate recognition by IL-2R expressing cells.
Methods: We used transmission electron microscopy and flow cytometry to evaluate physical characteristics of the system and immunodeppressed CBA mice for toxicological, pharmacodynamic and pharmacokinetic parameters.
Results: Our results show that liposomes in our system have a unilamellar structure, small enough to be easily internalized by tumor cells, a viscosity similar to water, and are stable over a wide range of light, pH and temperature conditions, which provide them with convenient properties for pharmaceutical dosage forms, and storage stability. By using an animal model of immunodeppressed CBA mice induced to form tumors derived from cervical cancer human cells, we show that our liposomes are non-toxic even at very high doses of liposome bound IL-2 molecules, and that far lower doses are very effective in significantly reducing the tumor burden. Our system has the same antitumor effect than free IL-2, but in the absence of extremely high toxicity associated with this molecule when administrated systemically, and at a longer permanence in tissues.
Conclusion: Our results shows that our system has low toxicity, long tissue permanence, and high antitumor activity, thus we propose the possibility that our IL-2 nanocarrier system could be useful for anti-cancer therapy when tumor cells express the IL-2R.
Keywords: IL-2 and IL-2R, liposomes, nanocarrier system, pharmacokinetic and pharmacodynamic properties, toxicity, antitumor activity.
Graphical Abstract
Current Nanomedicine
Title:A Novel Nanocarrier System for Cancer Treatment
Volume: 6 Issue: 2
Author(s): María Teresa Corona-Ortega, Ramón Soto-Vázquez, Rosalva Rangel-Corona, Rosa María Huante-García, Leonor Aguilar-Santelises, Araceli García del Valle and Benny Weiss-Steider
Affiliation:
Keywords: IL-2 and IL-2R, liposomes, nanocarrier system, pharmacokinetic and pharmacodynamic properties, toxicity, antitumor activity.
Abstract: Background: We have designed and patented a novel nanocarrier system to specifically deliver IL-2 to tumor cells expressing the IL-2 receptor (IL-2R). In this work, we provide data of the physical characteristics of the system, such as size, complexity and viscosity, stability to light, pH and temperature, pharmacodynamic and pharmacokinetic parameters, as well as toxic and antitumor properties. The nanocarrier system consists of positively charged liposomes that present non-covalently bound IL-2 molecules on their external surface to facilitate recognition by IL-2R expressing cells.
Methods: We used transmission electron microscopy and flow cytometry to evaluate physical characteristics of the system and immunodeppressed CBA mice for toxicological, pharmacodynamic and pharmacokinetic parameters.
Results: Our results show that liposomes in our system have a unilamellar structure, small enough to be easily internalized by tumor cells, a viscosity similar to water, and are stable over a wide range of light, pH and temperature conditions, which provide them with convenient properties for pharmaceutical dosage forms, and storage stability. By using an animal model of immunodeppressed CBA mice induced to form tumors derived from cervical cancer human cells, we show that our liposomes are non-toxic even at very high doses of liposome bound IL-2 molecules, and that far lower doses are very effective in significantly reducing the tumor burden. Our system has the same antitumor effect than free IL-2, but in the absence of extremely high toxicity associated with this molecule when administrated systemically, and at a longer permanence in tissues.
Conclusion: Our results shows that our system has low toxicity, long tissue permanence, and high antitumor activity, thus we propose the possibility that our IL-2 nanocarrier system could be useful for anti-cancer therapy when tumor cells express the IL-2R.
Export Options
About this article
Cite this article as:
Corona-Ortega Teresa María, Soto-Vázquez Ramón, Rangel-Corona Rosalva, Huante-García María Rosa, Aguilar-Santelises Leonor, Valle García del Araceli and Weiss-Steider Benny, A Novel Nanocarrier System for Cancer Treatment, Current Nanomedicine 2016; 6 (2) . https://dx.doi.org/10.2174/2468187306999160427114000
DOI https://dx.doi.org/10.2174/2468187306999160427114000 |
Print ISSN 2468-1873 |
Publisher Name Bentham Science Publisher |
Online ISSN 2468-1881 |

- Author Guidelines
- Bentham Author Support Services (BASS)
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
Related Articles
-
Molecular Targeted Approaches to Cancer Therapy and Prevention Using Chalcones
Current Cancer Drug Targets Herb-drug Interactions Involving Drug Metabolizing Enzymes and Transporters
Current Drug Metabolism A Facile “Click Chemistry” Approach to Novel Flavonol Glycoconjugates and Their Cytotoxic Activity
Letters in Organic Chemistry Enzyme / Abzyme Prodrug Activation Systems: Potential Use in Clinical Oncology
Current Pharmaceutical Design Pleiotrophin as a Possible New Target for Angiogenesis-Related Diseases and Cancer
Recent Patents on Anti-Cancer Drug Discovery Topical Application of <i>In Vitro</i> Transcribed mRNA to the Airways as a Novel Gene Therapy Approach for the Treatment of Cystic Fibrosis
Clinical Immunology, Endocrine & Metabolic Drugs (Discontinued) Multifunctional Anti-Cancer Nano-Platforms are Moving to Clinical Trials
Current Drug Metabolism Lobaplatin Induces Pyroptosis in Cervical Cancer Cells via the Caspase-3/GSDME Pathway
Anti-Cancer Agents in Medicinal Chemistry Innate Immunity and Vaccine Adjuvants: From Concepts to the Development of a Unique Adjuvant System AS04 Used for the Formulation of a Human Papillomavirus (HPV) Vaccine
Current Cancer Therapy Reviews Nutraceuticals for Promoting Longevity
Current Nutraceuticals The Dynamics of the Hypothalamic-Pituitary-Ovarian Axis, ReproductivePerformance and Sexuality Following Bariatric Surgery
Current Women`s Health Reviews Management of Fallopian Tube Cancer
Reviews on Recent Clinical Trials Current Constructs and Targets in Clinical Development for Antibody- Based Cancer Therapy
Current Drug Targets New Pyrano[2,3-d:6,5-d']dipyrimidine Derivatives-Synthesis, in vitro Cytotoxicity and Computational Studies
Anti-Cancer Agents in Medicinal Chemistry Biologic Agents in the Treatment of Psoriasis
Recent Patents on Inflammation & Allergy Drug Discovery Back to the Future: COX-2 Inhibitors for Chemoprevention and Cancer Therapy
Mini-Reviews in Medicinal Chemistry The Roles of miR-25 and its Targeted Genes in Development of Human Cancer
MicroRNA The Cyclin-Dependent Kinase Inhibitor p21CDKN1A as a Target of Anti-Cancer Drugs
Current Cancer Drug Targets New Molecular Targets of Anticancer Therapy – Current Status and Perspectives
Current Medicinal Chemistry Alternatives to Conventional Vaccines - Mediators of Innate Immunity
Current Drug Targets