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Journal ArticleDOI

PLGA-dendron nanoparticles enhance immunogenicity but not lethal antibody production of a DNA vaccine against anthrax in mice

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TLDR
Results indicate that the PLGA-C(18) dendriplex particles produced superior levels of anti-PA IgG antibodies in comparison to animals immunized with thePLGA- C(0) dendedriplex particle, and it is likely that the mice lack protection against lethal toxin and anthrax infection.
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This article is published in International Journal of Pharmaceutics.The article was published on 2007-03-01. It has received 48 citations till now. The article focuses on the topics: Bacillus anthracis.

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Nonviral Vectors for Gene Delivery

TL;DR: Two nonviral gene delivery systems using either biodegradable poly(D,Llactide-co-glycolide) (PLG) nanoparticles or cell penetrating peptide (CPP) complexes have been designed and studied using A549 human lung epithelial cells.
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Current advances in research and clinical applications of PLGA-based nanotechnology

TL;DR: More recent successes of applying PLGA-based nanotechnologies and tools in medicine-related applications are presented and the possible mechanisms, diagnosis and treatment effects of PLGA preparations and devices are focused on.
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Cationic polymers and their therapeutic potential

TL;DR: The most recent scientific advances in cationic polymers and their derivatives not only for gene delivery purposes but also for various alternative therapeutic applications are reviewed.
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Design of biocompatible dendrimers for cancer diagnosis and therapy: current status and future perspectives

TL;DR: This critical review focuses on the design of biocompatible dendrimer-based nanoplatforms for targeted cancer diagnosis and therapy and theBiocompatibility aspects of d endrimers such as nanotoxicity, long-term circulation, and degradation are discussed.
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A Single-Dose PLGA Encapsulated Protective Antigen Domain 4 Nanoformulation Protects Mice against Bacillus anthracis Spore Challenge

TL;DR: The possibility of the development of a single-dose and adjuvant-free protective antigen based anthrax vaccine in the form of PAD4-NP is demonstrated for the first time.
References
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Journal ArticleDOI

Immunotherapeutic uses of CpG oligodeoxynucleotides

TL;DR: Ongoing clinical studies indicate that CpG ODN use is safe in humans, and that they modulate the immune response to co-administered allergens and vaccines.
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Biodegradable poly(lactic-co-glycolic acid) microparticles for injectable delivery of vaccine antigens

TL;DR: This review examines several impediments to PLGA microparticle development, such as PLGA-encapsulated antigen instability and deficiency of animal models in predicting human response, and describes new trends in overcoming these important issues.
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Bacterial DNA Induces Murine Interferon-γ Production by Stimulation of Interleukin-12 and Tumor Necrosis Factor-α

TL;DR: Results indicate that the stimulation of IFN-γ production by bacterial DNA is mediated by IL-12 and TNF-α and point to macrophages/monocytes as targets of action of this macromolecule.
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Poly(lactide-co-glycolide) microparticles for the development of single-dose controlled-release vaccines.

TL;DR: The adjuvant effect of PLG microparticles are discussed, and their potential for the development of single-dose vaccines through the use of controlled-release technology is discussed.
Journal ArticleDOI

Efficacy of a human anthrax vaccine in guinea pigs, rabbits, and rhesus macaques against challenge by Bacillus anthracis isolates of diverse geographical origin

TL;DR: It is demonstrated that, although AVA confers variable protection against different B. anthracis isolates in guinea pigs, it is highly protective against these same isolate in both rabbits and rhesus macaques.
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