Targeting strategies for improving the efficacy of nanomedicine in oncology (original) (raw)

Nanoparticles as carriers for drug delivery in cancer

Artificial Cells, Nanomedicine, and Biotechnology

Cancer nanotherapeutics are swiftly progressing and are being applied to solve several limitations of conventional drug delivery systems such as non-specific biodistribution and targeting, lack of water solubility and poor oral bioavailability. Advances in protein engineering and materials science have contributed to novel nanoscale targeting approaches that may bring new hope to cancer patients. Several therapeutic nanocarriers have been approved for clinical use. Nanoparticles have been designed for optimal size and surface characteristics to improve their biodistribution and to increase their circulation time in the bloodstream. By selectively using the unique pathophysiology of tumours, such as their enhanced permeability and retention effect nanotherapeutics are able to carry loaded active drug to cancer cells. In addition to this passive targeting mechanism, active targeting strategies using ligands or antibodies directed against selected tumour targets magnify the specificity of these therapeutic nanoparticles. Drug resistance, another obstacle can also be overcome or reduced by using nanoparticles. Multifunctional and multiplex nanoparticles are now being actively investigated and are on the horizon as the next generation of nanoparticles, facilitating personalized and tailored cancer treatment.

A Review on Nanocarriers for Cancer Targeted Drug Delivery

2020

Nanoparticles in the drugs are useful for the treatment of cancer due to their unique properties and can act as drug carriers in different ways. Unlike the traditional chemotherapy, the entrance of nanotechnology enabled wide applications in treatment of cancer. Although nanoparticles provides safe and effective drug delivery systems but the factor of toxicity still limits the utilisation of several nanoparticles. The properties of nanodrug carriers are controllable by various factors. The use of nanoparticles in cancer therapy by drug delivery and their advantages as been reviewed.

Nanotechnology in Cancer Drug Delivery and Selective Targeting

ISRN Nanotechnology, 2014

Nanoparticles are rapidly being developed and trialed to overcome several limitations of traditional drug delivery systems and are coming up as a distinct therapeutics for cancer treatment. Conventional chemotherapeutics possess some serious side effects including damage of the immune system and other organs with rapidly proliferating cells due to nonspecific targeting, lack of solubility, and inability to enter the core of the tumors resulting in impaired treatment with reduced dose and with low survival rate. Nanotechnology has provided the opportunity to get direct access of the cancerous cells selectively with increased drug localization and cellular uptake. Nanoparticles can be programmed for recognizing the cancerous cells and giving selective and accurate drug delivery avoiding interaction with the healthy cells. This review focuses on cell recognizing ability of nanoparticles by various strategies having unique identifying properties that distinguish them from previous antic...

Nanocarriers for Cancer-Targeted Drug Delivery: Review and Challenges

2020

From the past decade, researchers have seen the potential application of nanotechnology in the field of cancer-targeted drug delivery. Nanoparticle-based chemical moieties such as polymeric based nanoparticles, dendrimers, polymersomes, liposomes, nano micelles, metal nanoparticles, carbon nanotubes (CNTs), etc. Due to their exclusive properties such as tunable surface chemistry, ability to penetrate cells, stimuli-sensitization they could be designed as per the targeted tissue or cells of the tumor. This review provides an insight into the development of nanomedicine with the help of different nanocarriers for cancer/tumor-targeted drug delivery. But apart from having desired flexibility in the development of nanocarrier based drug compound, it has some drawbacks/challenges. The review will also discuss

I IN ND DO O A AM ME ER RI IC CA AN N J JO OU UR RN NA AL L O OF F P PH HA AR RM MA AC CE EU UT TI IC CA AL L S SC CI IE EN NC CE ES S PASSIVE AND ACTIVE TUMOR TARGETING OF NANO CARRIERS FOR ANTI-CANCER DRUG DELIVERY-A REVIEW

Because of the particular characteristics of the tumor microenvironment and tumor angiogenesis, it is possible to design drug delivery systems that specifically target anti-cancer drugs to tumors. Most of the conventional chemotherapeutic agents have poor pharmacokinetics profiles and are distributed non-specifically in the body leading to systemic toxicity associated with serious side effects. Therefore, the development of drug delivery systems able to target the tumor site is becoming a real challenge that is currently addressed. Nanomedicine can reach tumor passively through the leaky vasculature surrounding the tumors by the Enhanced Permeability and Retention effect whereas ligands grafted at the surface of nanocarriers allow active targeting by binding to the receptors overexpressed by cancer cells or angiogenic endothelial cells. This review is divided into two parts: the first one describes the tumor microenvironment and the second one focuses on the exploitation and the understanding of these characteristics to design new drug delivery systems targeting the tumor. Delivery of conventional chemotherapeutic anti-cancer drugs is mainly discussed.

Nanocarriers in advanced drug targeting: setting novel paradigm in cancer therapeutics

2017

Cancer has been growing nowadays consequently high number of death ascertained worldwide. The medical intervention involves chemotherapy, radiation therapy and surgical removal. This conventional technique lacking targeting potential and harm the normal cells. In drug treatment regimen, the combination therapy is preferred than single drug treatment module due to higher internalization of chemotherapeutics in the cancer cells both by enhance permeation retention effect and by direct cell apoptosis. The cancer therapeutics involves different methodologies of delivering active moiety to the target site. The active and passive transport mode of chemotherapeutic targeting utilizes advance nanocarriers. The nanotechnological strategic treatment applying advance nanocarrier greatly helps in mitigating the cancer prevalence. The nanocarrier-incorporating nanodrug directed for specific area appealed scientist across the globe and issues to be addressed in this regard. Therefore, various techniques and approaches invented to meet the objectives. With the advances in nanomedicine and drug delivery, this review briefly focused on various modes of nanodrug delivery including nanoparticles, liposomes, dendrimer, quantum dots, carbon nanotubes, metallic nanoparticles, nanolipid carrier (NLC), gold nanoshell, nanosize cantilevers and nanowire that looks promising and generates a novel horizon in cancer therapeutics.

Target Nanoparticles: An Appealing Drug Delivery Platform

Journal of Nanomedicine & Nanotechnology, 2011

Over recent years advancement in nanoparticles drug delivery is widely expected to change the landscape of pharmaceutical and biotechnology industries for the foreseeable future. Nanoparticles are solid colloidal matrix-like particles made of polymers or lipids. Generally administered by the intravenous route like liposome's, they have been developed for the targeted delivery of therapeutic or imaging agents. Nanomaterials have emerged as a promising strategy in delivering therapeutic molecules effectively to diseased sites. Furthermore, most nonmaterial surfaces can be decorated with targeting ligands, enhancing their ability to home to diseased tissues through multivalent interactions with tissue-specific receptors. Thus, targeted therapy provides a means to circumvent the toxicities and lack of treatment response of conventional systemic chemotherapy. Targeted liposome's, micelles, carbon nanotubes and dendrimers incorporated with therapeutic molecules have displayed impressive anticancer effects in animal studies, and these nanomaterials are considered to be close to clinical translation due to their biocompatibility. These carriers are designed in such a way that they are independent in the environments and selective at the pharmacological site. In addition, these nanomaterials have the capability to reverse multidrug resistance a major problem in chemotherapy. Finally, tumor-homing nanosystems that amplify tumor homing can also improve the delivery of compounds to tumors, providing imaging and therapeutic options that were previously unavailable. Journal of Nanomedicine & Nanotechnology J o u rna l of N a n o m ed icine & N a n o te chnolo g y

Nanoparticles, Promising Carriers in Drug Targeting: A Review

Current Drug Therapy, 2011

Nanotechnology (derived from the Greek word nano meaning dwarf) is generally defined as the science and engineering of constructing and assembling objects on a scale smaller than one hundred nanometers. Nanotechnology is a multidisciplinary scientific field undergoing explosive development. Nanoparticles are colloidal systems of submicron (< 1 μM) size that can be constructed from a large variety of materials in a large variety of compositions. Commonly defined nanoparticle vectors include: liposomes, micelles, dendrimers, solid lipid nanoparticles, metallic nanoparticles, semiconductor nanoparticles and polymeric nanoparticles. Nanoparticles have been considered as effective delivery systems for many reasons including: (i) sufficient physical and biological stability that may facilitate drug entrapment and controlled release; (ii) good tolerability of the components; (iii) simplicity of the formulation processing; and (iv) possibility of scaling up the formulation process. Therefore, nanoparticles have been extensively employed to deliver drugs, genes, vaccines and diagnostics into specific cells/tissues. Site-specific delivery of drug receives a lot of attention because it can reduce drug toxicity and increase therapeutic effects. To solve the problem of site-specific targeting for the colloidal systems, some authors have attempted to increase the tissue specificity of colloidal drug carriers by coupling targeting agents. In recent years the improvement of drug therapy in terms of a more controlled body distribution to reduce side effects was focused. Different new drug carrier systems in the micro-and nanometer size range were generated to overcome these problems. In principle, four different schemes of drug targeting are conceivable: firstly, a direct application of the drug to the pathological site which in most cases is not possible; secondly, passive targeting depending on carrier system accumulation in areas with leaky vasculature showing an enhanced permeability and retention effect (EPR-effect); thirdly, employment of physical effects like varying pH values, differences in temperature or magnetic systems, and finally as the most promising strategy the use of specific vector molecules such as antibodies representing the most universal approach. The objective of this review was to emphasize on drug targeting and various approaches of drug targeting through nanoparticles.

Application of nano-based systems for drug delivery and targeting: a review

Journal of Nanoparticle Research, 2020

Over the last decades, magnificent progress in the field of nanopharmaceuticals mostly with sizes smaller than 100 nm has led to the development of novel delivery systems and brightened the hope of finding new approaches to combat threatening diseases including cancer. So far, numerous efforts have been made to develop appropriate delivery systems with favorable features such as acceptable toxicity profile, high cellular uptake, low immunogenicity, and stable physicochemical properties along with distribution of the therapeutic molecule specifically to the site of action, without affecting healthy organs and tissues. Non-viral delivery systems have always been suitable options for delivery purposes. Polymers, liposomes, and inorganic delivery systems are all of the available choices in non-viral delivery systems, with each possessing their own advantages and pitfalls. This current review presents the recent advances about the application of various nonviral nanocarriers in the delivery of diverse therapeutic agents especially in cancer treatment. Targeting ligands as an important part of designing targeted nanocarriers to the site of interest or intra-cellular environment and opportunities and challenges of nano-based systems for drug and gene delivery are also discussed.

Therapeutic Nanoparticles for Drug Delivery in Cancer

Cancer nanotherapeutics are rapidly progressing and are being implemented to solve several limitations of conventional drug delivery systems such as nonspecific biodistribution and targeting, lack of water solubility, poor oral bioavailability, and low therapeutic indices. To improve the bio-distribution of cancer drugs, nanoparticles have been designed for optimal size and surface characteristics to increase their circulation time in the bloodstream. They are also able to carry their loaded active drugs to cancer cells by selectively using the unique pathophysiology of tumors, such as their enhanced permeability and retention effect and the tumor microenvironment. In addition to this passive targeting mechanism, active targeting strategies using ligands or antibodies directed against selected tumor targets amplify the specificity of these therapeutic nanoparticles. Drug resistance, another obstacle that impedes the efficacy of both molecularly targeted and conventional chemotherapeutic agents, might also be overcome, or at least reduced, using nanopar-ticles. Nanoparticles have the ability to accumulate in cells without being recognized by P-glycoprotein, one of the main mediators of multidrug resistance, resulting in the increased intra-cellular concentration of drugs. Multifunctional and multiplex nanoparticles are now being actively investigated and are on the horizon as the next generation of nanoparticles, facilitating personal-ized and tailored cancer treatment.