Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Modified-Release Drug Delivery Systems: Site-Targeted01:24

Modified-Release Drug Delivery Systems: Site-Targeted

Site-targeted drug delivery systems enhance therapeutic efficacy while minimizing systemic toxicity and treatment costs. Unlike conventional methods, these systems ensure precise drug delivery, improving bioavailability and reducing side effects. Targeted drug delivery is classified into three levels. First-order targeting directs drugs to the capillary beds of specific organs or tissues. Second-order targets specific cell types, such as tumor cells, using receptor-mediated interactions.
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
Site-Targeted Drug Delivery Systems: Polymeric Carriers01:24

Site-Targeted Drug Delivery Systems: Polymeric Carriers

Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...
Treatment Resistent Cancers02:56

Treatment Resistent Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
Drug Delivery: Overview01:16

Drug Delivery: Overview

The selection of a drug's delivery route depends upon its physicochemical properties, including lipid or water solubility and ionization, as well as the therapeutic requirement, such as immediate or sustained effect. These routes can be divided into three primary categories: enteral, parenteral, and topical.
Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the gastrointestinal...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Codelivery of Cell Apoptosis AVPIAQ Peptide and Doxorubicin for Synergistic Cancer Therapy.

ACS applied bio materials·2025
Same author

Targeted Drug Delivery Strategies for the Treatment of Hepatocellular Carcinoma.

Molecules (Basel, Switzerland)·2024
Same author

Enzyme-Responsive Micelles with High Drug-Loading Capacity for Antitumor Therapy.

Macromolecular rapid communications·2024
Same author

Advances in 2,3-Dimethylmaleic Anhydride (DMMA)-Modified Nanocarriers in Drug Delivery Systems.

Pharmaceutics·2024
Same author

An MMP-2 sensitive and reduction-responsive prodrug amphiphile for actively targeted therapy of cancer by hierarchical cleavage.

Chemical communications (Cambridge, England)·2023
Same author

Intelligent Drug Delivery by Peptide-Based Dual-Function Micelles.

International journal of molecular sciences·2022

Related Experiment Video

Updated: May 14, 2026

Nanoparticle Delivery of an Oligonucleotide Payload in a Glioblastoma Multiforme Animal Model
09:02

Nanoparticle Delivery of an Oligonucleotide Payload in a Glioblastoma Multiforme Animal Model

Published on: September 27, 2024

Nuclear-Targeted Drug Delivery Systems for Cancer Therapy: Advances, and Challenges.

Yonghui Liu1, Yanan Wu1,2, Yifan Wu1

  • 1School of Chemistry, Tiangong University, Tianjin 300387, China.

Molecules (Basel, Switzerland)
|May 13, 2026
PubMed
Summary
This summary is machine-generated.

Nuclear-targeted drugs offer promising tumor therapy, but biological barriers limit their effectiveness. This review explores advanced delivery strategies to enhance drug entry into the nucleus for improved cancer treatment.

Keywords:
anticancercontrolled releasedrug delivery systemnuclear-targetedtumor therapy

More Related Videos

A Comprehensive Procedure to Evaluate the In Vivo Performance of Cancer Nanomedicines
07:59

A Comprehensive Procedure to Evaluate the In Vivo Performance of Cancer Nanomedicines

Published on: March 4, 2017

Related Experiment Videos

Last Updated: May 14, 2026

Nanoparticle Delivery of an Oligonucleotide Payload in a Glioblastoma Multiforme Animal Model
09:02

Nanoparticle Delivery of an Oligonucleotide Payload in a Glioblastoma Multiforme Animal Model

Published on: September 27, 2024

A Comprehensive Procedure to Evaluate the In Vivo Performance of Cancer Nanomedicines
07:59

A Comprehensive Procedure to Evaluate the In Vivo Performance of Cancer Nanomedicines

Published on: March 4, 2017

Area of Science:

  • Oncology
  • Drug Delivery
  • Nanotechnology

Background:

  • Nuclear-targeted drugs are crucial for cancer therapy, interacting with DNA or enzymes.
  • Biological barriers in vivo significantly hinder drug delivery to the nucleus, reducing therapeutic efficacy.
  • The nucleus is a primary target for anticancer agents due to its role in DNA replication and transcription.

Purpose of the Study:

  • To systematically review advanced delivery strategies for nuclear-targeted drug systems.
  • To explore the therapeutic applications of these systems in oncology.
  • To analyze current challenges and future opportunities in developing intelligent nuclear delivery platforms.

Main Methods:

  • Literature review of advanced drug delivery systems for nuclear targeting.
  • Analysis of therapeutic applications in various cancer models.
  • Discussion of challenges and future prospects for nuclear drug delivery.

Main Results:

  • Various advanced delivery strategies are being developed to overcome biological barriers.
  • Nuclear-targeted drug systems show potential in diverse oncological applications.
  • Significant challenges remain in achieving efficient and specific nuclear drug delivery.

Conclusions:

  • Advanced delivery systems are essential for overcoming barriers to nuclear drug targeting in cancer therapy.
  • Further research is needed to develop next-generation intelligent nuclear delivery platforms for enhanced oncology outcomes.
  • Optimizing drug delivery to the nucleus holds significant promise for improving cancer treatment efficacy.