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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1186/s11671-021-03628-6.

Title:
Nanoparticles for Cancer Therapy: Current Progress and Challenges | Discover Nano
Description:
Cancer is one of the leading causes of death and morbidity with a complex pathophysiology. Traditional cancer therapies include chemotherapy, radiation therapy, targeted therapy, and immunotherapy. However, limitations such as lack of specificity, cytotoxicity, and multi-drug resistance pose a substantial challenge for favorable cancer treatment. The advent of nanotechnology has revolutionized the arena of cancer diagnosis and treatment. Nanoparticles (1–100 nm) can be used to treat cancer due to their specific advantages such as biocompatibility, reduced toxicity, more excellent stability, enhanced permeability and retention effect, and precise targeting. Nanoparticles are classified into several main categories. The nanoparticle drug delivery system is particular and utilizes tumor and tumor environment characteristics. Nanoparticles not only solve the limitations of conventional cancer treatment but also overcome multidrug resistance. Additionally, as new multidrug resistance mechanisms are unraveled and studied, nanoparticles are being investigated more vigorously. Various therapeutic implications of nanoformulations have created brand new perspectives for cancer treatment. However, most of the research is limited to in vivo and in vitro studies, and the number of approved nanodrugs has not much amplified over the years. This review discusses numerous types of nanoparticles, targeting mechanisms, and approved nanotherapeutics for oncological implications in cancer treatment. Further, we also summarize the current perspective, advantages, and challenges in clinical translation.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Health & Fitness
  • Education

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Link.springer.com Make Money? {💾}

We can't tell how the site generates income.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

cancer, article, google, scholar, nps, cas, drug, cells, nanoparticles, therapy, tumor, targeting, delivery, resistance, cell, treatment, target, clinical, immunotherapy, drugs, system, breast, size, chemotherapy, targeted, nanotechnology, effect, nanoparticle, therapeutic, gene, shown, doxorubicin, zhang, liu, sci, wang, toxicity, effects, immune, properties, res, blood, paclitaxel, httpsdoiorgs, yang, due, studies, surface, cellular, biological,

Topics {✒}

%20facts%20%26%20figures%20annual%20report%20provides%3a%201 park cancer-facts-figures/cancer-facts-figures-2021 /science/article/pii/s1631070511001538 laurent avidity-based pd-l1 antagonist transferrin-modified peg-phosphatidyl-ethanolamine anti-igg-peg-au nanoparticles org/research/cancer-facts-statistics/ ïżœhypoxia-inducible factor 1α ïżœanti-her2 functionalized gold ïżœspermine-modified acetylated dextran quantum dot-aptamer conjugates nanocarrier-mediated subcellular targeting phb-pdmaema cationic polyester lithium-ion polymer batteries folate-conjugated gold nanoparticle ïżœpi3k/akt/mtor pathway” microrna-smad-bmp-2 circuit ïżœmyeloid-derived suppressor cells dehydration-rehydration liposomal system nanoparticle-mediated cellular response anti-tumor multidrug resistance planetary ball milled drug-delivery/andronescu/978-0-323-46143-6 bernardi phase change micro/nanoparticles single-chain antibody fragments mhc-antigen complexes directly obstructing “cd47-sirpα pathways” sp2-hybridized carbon sheet ph-sensitive polymeric nanoparticles hpma copolymer-dach-platinate typically nanometer-scale semiconductors treat transthyretin-mediated amyloidosis multi-drug resistance pose hif-1α/cd73 axis triggering pro-apoptotic factors ÎČ-cyclodextrin nanosponges loaded nanoparticle-based cancer drug exhibit anti-tumor effects approved liposome-based formulations anti-egfr-peg-aunps hpma copolymer-doxorubicin galactosamine artificial antigen-presenting cells hybridizing pb-activated dnazyme multidrug transporters p-glycoprotein ïżœp388/adr leukemia cells” article download pdf drug-resistant tumor models fluorescent single-walled cnt pump-mediated drug resistance atp-hydrolyzing subunits/domains

Questions {❓}

  • Awasthi R, Pant I, Kulkarni G, Satiko Kikuchi I, de Jesus Andreoli Pinto T, Dua K, Ramana Malipeddi V (2016) Opportunities and challenges in nano-structure mediated drug delivery: Where do we stand?
  • Hu Y, Gaillard PJ, de Lange E, Hammarlund-Udenaes M (2019) Targeted brain delivery of methotrexate by glutathione PEGylated liposomes: How can the formulation make a difference?
  • Pederzoli F, Tosi G, Vandelli MA, Belletti D, Forni F, Ruozi B (2017) Protein corona and nanoparticles: How can we investigate on?

Schema {đŸ—ș}

WebPage:
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         headline:Nanoparticles for Cancer Therapy: Current Progress and Challenges
         description:Cancer is one of the leading causes of death and morbidity with a complex pathophysiology. Traditional cancer therapies include chemotherapy, radiation therapy, targeted therapy, and immunotherapy. However, limitations such as lack of specificity, cytotoxicity, and multi-drug resistance pose a substantial challenge for favorable cancer treatment. The advent of nanotechnology has revolutionized the arena of cancer diagnosis and treatment. Nanoparticles (1–100 nm) can be used to treat cancer due to their specific advantages such as biocompatibility, reduced toxicity, more excellent stability, enhanced permeability and retention effect, and precise targeting. Nanoparticles are classified into several main categories. The nanoparticle drug delivery system is particular and utilizes tumor and tumor environment characteristics. Nanoparticles not only solve the limitations of conventional cancer treatment but also overcome multidrug resistance. Additionally, as new multidrug resistance mechanisms are unraveled and studied, nanoparticles are being investigated more vigorously. Various therapeutic implications of nanoformulations have created brand new perspectives for cancer treatment. However, most of the research is limited to in vivo and in vitro studies, and the number of approved nanodrugs has not much amplified over the years. This review discusses numerous types of nanoparticles, targeting mechanisms, and approved nanotherapeutics for oncological implications in cancer treatment. Further, we also summarize the current perspective, advantages, and challenges in clinical translation.
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      headline:Nanoparticles for Cancer Therapy: Current Progress and Challenges
      description:Cancer is one of the leading causes of death and morbidity with a complex pathophysiology. Traditional cancer therapies include chemotherapy, radiation therapy, targeted therapy, and immunotherapy. However, limitations such as lack of specificity, cytotoxicity, and multi-drug resistance pose a substantial challenge for favorable cancer treatment. The advent of nanotechnology has revolutionized the arena of cancer diagnosis and treatment. Nanoparticles (1–100 nm) can be used to treat cancer due to their specific advantages such as biocompatibility, reduced toxicity, more excellent stability, enhanced permeability and retention effect, and precise targeting. Nanoparticles are classified into several main categories. The nanoparticle drug delivery system is particular and utilizes tumor and tumor environment characteristics. Nanoparticles not only solve the limitations of conventional cancer treatment but also overcome multidrug resistance. Additionally, as new multidrug resistance mechanisms are unraveled and studied, nanoparticles are being investigated more vigorously. Various therapeutic implications of nanoformulations have created brand new perspectives for cancer treatment. However, most of the research is limited to in vivo and in vitro studies, and the number of approved nanodrugs has not much amplified over the years. This review discusses numerous types of nanoparticles, targeting mechanisms, and approved nanotherapeutics for oncological implications in cancer treatment. Further, we also summarize the current perspective, advantages, and challenges in clinical translation.
      datePublished:2021-12-05T00:00:00Z
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         Nanoparticles
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         Cellular targeting
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         Nanoscale Science and Technology
         Nanochemistry
         Molecular Medicine
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      address:
         name:GenLab Biosolutions Private Limited, Bangalore, India
         type:PostalAddress
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      affiliation:
            name:GenLab Biosolutions Private Limited
            address:
               name:Department of Life Sciences, GenLab Biosolutions Private Limited, Bangalore, India
               type:PostalAddress
            type:Organization
      name:Sameer Quazi
      affiliation:
            name:GenLab Biosolutions Private Limited
            address:
               name:GenLab Biosolutions Private Limited, Bangalore, India
               type:PostalAddress
            type:Organization
      name:Tomasz M. KarpiƄski
      url:http://orcid.org/0000-0001-6599-9204
      affiliation:
            name:PoznaƄ University of Medical Sciences
            address:
               name:Chair and Department of Medical Microbiology, PoznaƄ University of Medical Sciences, PoznaƄ, Poland
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Life Sciences, GenLab Biosolutions Private Limited, Bangalore, India
      name:GenLab Biosolutions Private Limited, Bangalore, India
      name:Chair and Department of Medical Microbiology, PoznaƄ University of Medical Sciences, PoznaƄ, Poland

External Links {🔗}(499)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
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  • Prism.js

CDN Services {📩}

  • Crossref

6.04s.