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Nanoparticles as drug delivery systems

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TLDR
Various nanostructures, including liposomes, polymers, dendrimers, silicon or carbon materials, and magnetic nanoparticles, have been tested as carriers in drug delivery systems and their connections with drugs are analyzed.
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This article is published in Pharmacological Reports.The article was published on 2012-09-01 and is currently open access. It has received 1007 citations till now. The article focuses on the topics: Targeted drug delivery & Drug carrier.

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Polymer-based nanocapsules for drug delivery

TL;DR: A comparative analysis is given of the size, zeta-potential, dispersion pH, shell thickness, encapsulation efficiency, active substance release, stability and in vivo and in vitro pharmacological performances, which allows establishing criteria for selecting a method for preparation of nanocapsules according to its advantages, limitations and behaviours as a drug carrier.
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Monodisperse Gold Nanotriangles: Size Control, Large-Scale Self-Assembly, and Performance in Surface-Enhanced Raman Scattering

TL;DR: Extended monolayers of Au nanotriangles show promising performance as surface-enhanced Raman scattering substrates, as demonstrated for thiophenol detection.
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Therapeutic efficacy of nanoparticles and routes of administration

TL;DR: The most commonly used nanomaterials, their core properties and how surface functionalization would facilitate competent delivery of drugs or therapeutic molecules are explained to facilitate straightforward perception of nanocarrier design, routes of various nanoparticle administration and the challenges associated with each drug delivery method.
Journal ArticleDOI

The biological activities, chemical stability, metabolism and delivery systems of quercetin: A review

TL;DR: In this paper, a review of the biological activities, chemical stability, metabolism and toxicity of quercetin and different delivery systems for quercET were discussed, including lipid-based carriers, nanoparticles, inclusion complexes, micelles and conjugates-based encapsulation.
References
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Journal ArticleDOI

Biodegradable nanoparticles for drug and gene delivery to cells and tissue

TL;DR: Based on the above mechanism, various potential applications of nanoparticles for delivery of therapeutic agents to the cells and tissue are discussed.
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Biodegradable polymeric nanoparticles based drug delivery systems

TL;DR: The impact of nanoencapsulation of various disease related drugs on biodegradable nanoparticles such as PLGA, PLA, chitosan, gelatin, polycaprolactone and poly-alkyl-cyanoacrylates is highlighted.
Journal ArticleDOI

Carbon nanotubes introduced into the abdominal cavity of mice show asbestos-like pathogenicity in a pilot study.

TL;DR: Exposing the mesothelial lining of the body cavity of mice to long multiwalled carbon nanotubes results in asbestos-like, length-dependent, pathogenic behaviour, including inflammation and the formation of lesions known as granulomas.
Journal ArticleDOI

Mesoporous silica nanoparticles as controlled release drug delivery and gene transfection carriers

TL;DR: This review highlights the recent research developments of a series of surface-functionalized mesoporous silica nanoparticle (MSN) materials as efficient drug delivery carriers and envision that these MSN-based systems have a great potential for a variety of drug delivery applications.
Journal ArticleDOI

Pulmonary Toxicity of Single-Wall Carbon Nanotubes in Mice 7 and 90 Days After Intratracheal Instillation

TL;DR: Results show that, for the test conditions described here and on an equal-weight basis, if carbon nanotubes reach the lungs, they are much more toxic than carbon black and can be more Toxic than quartz, which is considered a serious occupational health hazard in chronic inhalation exposures.
Related Papers (5)
Frequently Asked Questions (15)
Q1. What is the role of nanocarriers in the EPR?

In addition, the design of nanocarriers as active targeting systems may involve the coupling of recognition molecules as surface receptors which are able to initiate endocytosis, and hence to increase cell internalization in contrast to simple accumulation [81]. 

This chapter presents a review on the design of nanoparticles which have been proposed as drug delivery systems in biomedicine. It will begin with a brief historical review of nanotechnology including the most common types of nanoparticles ( metal nanoparticles, liposomes, nanocrystals and polymeric nanoparticles ) and their advantages as drug delivery systems. Next, the nanoparticle design principles and the routes of administration of nanoparticles ( parental, oral, pulmonary and transdermal ) are discussed. 

The properties of nanoparticles that affect their removal are mainly based on size, shape, composition, charge, and surface chemistry. 

Controlled release is especially beneficial for those drugs whose half-life in the blood is relatively low due to a high rate of metabolism and elimination by the body. 

The justification for the use of nanoparticles as drug delivery systems lies in at least three mechanisms: (i) Enhanced Penetration and Retention (EPR) of nanoparticles in solid tumors; (ii) The possibility of transporting insoluble drugs in the blood through stable colloidal systems and (iii) the controlled release thereof. 

Particularly in the field of medicine, nanotechnology has the potential to generate a significant impact on human health, being able to improve the diagnosis, prevention and treatment of diseases. 

Total blood flow must pass through the liver, making it a central organ to monitor the blood for endogenous, foreign substances and particles that must be removed for physiological reasons. 

despite the great boom in metallic nanoparticles due to their long history and simplicity in terms of their synthesis, they present toxicity problems in prolonged use as they cannot be biodegraded [29–31]. 

a relevant question in the use of nanoparticles in humans is how these biological systems can eliminate nanoparticles once their functions have been fulfilled. 

The researchers concluded that the particles showed a high aerosolization performance through in vitro lung deposition measurement, which is at the level of commercially available dry powder inhalers. 

This evasion of the immune system tries to increase the circulation time of the nanoparticles in the body and, consequently, the chances that they find the target tissue while they circulate through the bloodstream. 

Since then and until April 2016, more than 50 nanomedicines of different kinds have been approved by the FDA and this is expected to be only the beginning of the near future [15]. 

At present, there have been technological advances that have managed to use various natural or synthetic lipids, as well as surfactants to modify the physicochemical properties of liposomes, giving rise to the second and third generation of them [36]. 

From this point of view, nanoparticle engineering is based on “programming” with predetermined instructions the self-assembly of atoms or molecules in such a way that the desired nanoparticles are the final product. 

molecular docking studies propose the reuse of these nanoparticles to combat the current global pandemic of SARS-CoV-2 [28].