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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.
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...
Transdermal Drug Delivery Systems01:18

Transdermal Drug Delivery Systems

Transdermal drug delivery systems (TDDS) enable the controlled release of drugs across the skin into systemic circulation. They are particularly advantageous for drugs with short half-lives or narrow therapeutic indices, as they maintain consistent plasma concentrations and reduce the risk of subtherapeutic or toxic levels.TDDS are categorized into monolithic, reservoir, and mixed systems. Monolithic systems embed the drug in a polymer matrix, where diffusion governs release. Reservoir systems...
Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

Rate-programmed drug delivery systems release drugs in a controlled manner to maintain therapeutic levels. Three main designs include reservoir, matrix, and hybrid systems.Reservoir systems consist of a drug core enclosed within a membrane that controls drug release. In non-swelling reservoir systems, polymers like ethyl cellulose or polymethacrylates are used. These do not hydrate in aqueous media and control release through membrane thickness, porosity, or insolubility. This type includes...
Intrauterine Drug Delivery Systems01:21

Intrauterine Drug Delivery Systems

Controlled-release systems for intravaginal and intrauterine drug delivery have been developed primarily for the administration of contraceptive steroid hormones. These delivery routes circumvent first-pass hepatic metabolism, thereby enhancing bioavailability and allowing for reduced systemic dosages compared to oral administration. Such approaches contribute to improved therapeutic efficacy and patient compliance, particularly in long-term contraceptive regimens.Intravaginal Drug Delivery...
Modified-Release Drug Delivery Systems: Classification01:23

Modified-Release Drug Delivery Systems: Classification

Modified-release drug delivery systems improve drug efficacy and minimize side effects by controlling the rate and location of drug release. These systems fall into three categories: rate-programmed, stimuli-activated, and site-targeted.Rate-programmed systems release drugs at a predetermined rate, maintaining consistent therapeutic levels and reducing fluctuations that could lead to toxicity or subtherapeutic effects. These systems use polymeric matrices, reservoir-based designs, or osmotic...

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Updated: May 15, 2026

Preparation and Characterization of Lipophilic Doxorubicin Pro-drug Micelles
09:56

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Published on: August 2, 2016

Paclitaxel drug delivery systems.

Zhiping Zhang1, Lin Mei, Si-Shen Feng

  • 1Huazhong University of Science & Technology, Tongji School of Pharmacy and National Engineering Research Center for Nanomedicine, Wuhan 430030, China.

Expert Opinion on Drug Delivery
|January 8, 2013
PubMed
Summary

Paclitaxel (PTX) drug delivery faces challenges due to poor water solubility. Nanotechnology offers solutions for enhanced solubility, targeted delivery, and reduced side effects of this crucial chemotherapy agent.

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Area of Science:

  • Pharmaceutical Nanotechnology
  • Drug Delivery Systems
  • Cancer Therapeutics

Background:

  • Paclitaxel (PTX) is a potent broad-spectrum chemotherapy agent.
  • Poor water solubility limits PTX clinical application and necessitates adjuvants with side effects.
  • Current PTX formulations exhibit suboptimal pharmacokinetics and biodistribution.

Purpose of the Study:

  • To review recent advancements in paclitaxel delivery systems.
  • To highlight nanotechnology-based solutions for PTX formulation challenges.
  • To explore methods for enhancing PTX solubility, permeability, stability, and targeted delivery.

Main Methods:

  • Review of various PTX delivery systems including prodrugs, micelles, liposomes, and nanoparticles.
  • Discussion of solid lipid nanoparticles, biodegradable polymer nanoparticles, dendrimers, and nanohydrogels.
  • Inclusion of paclitaxel-eluting stents as a delivery modality.

Main Results:

  • Nanotechnology offers solutions for PTX formulation and delivery challenges.
  • Nanocarriers demonstrate high drug encapsulation efficiency and cellular uptake.
  • Surface modification and appropriate sizing enable evasion of macrophage elimination.
  • Ligand conjugation facilitates targeted drug delivery.

Conclusions:

  • Pharmaceutical nanotechnology provides effective strategies to overcome PTX limitations.
  • Nanocarriers can significantly improve PTX therapeutic efficacy and reduce side effects.
  • Advancements in nanodelivery systems are transforming drug formulation and administration.