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 Experiment Videos

Mucosal drug delivery.

V H Lee1

  • 1Department of Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles 90089-9121, USA. vincentL@hsc.usc.edu

Journal of the National Cancer Institute. Monographs
|November 6, 2001
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Combination atezolizumab, bevacizumab, pemetrexed and carboplatin for metastatic EGFR mutated NSCLC after TKI failure.

Lung cancer (Amsterdam, Netherlands)·2021
Same author

Neurocardiology.

Handbook of clinical neurology·2017
Same author

Perfusion-based selection for endovascular reperfusion therapy in anterior circulation acute ischemic stroke.

AJNR. American journal of neuroradiology·2014
Same author

Prevalence and risk factors for aspirin and clopidogrel resistance in cerebrovascular stenting.

AJNR. American journal of neuroradiology·2007
Same author

Arginine vasopressin transport and metabolism in the pigmented rabbit conjunctiva.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2005
Same author

Gene expression, cell localization, and evolution of rodent submandibular gland androgen-binding protein.

European journal of morphology·2003
Same journal

Impact of WHO Classification of Tumours on cancer prevention, diagnosis, research, public health, and economics.

Journal of the National Cancer Institute. Monographs·2026
Same journal

Cancer epigenetics: unraveling etiology and mechanisms to advance prevention.

Journal of the National Cancer Institute. Monographs·2026
Same journal

Oncogenic infections: targets highly amenable to cancer prevention.

Journal of the National Cancer Institute. Monographs·2026
Same journal

The continuing importance of the IARC's international remit in cancer research.

Journal of the National Cancer Institute. Monographs·2026
Same journal

Environmental and occupational cancer: highlighting research contributions from the IARC on its 60th anniversary.

Journal of the National Cancer Institute. Monographs·2026
Same journal

Progress in identifying the preventable causes of human cancer: the experience of the IARC Monographs program.

Journal of the National Cancer Institute. Monographs·2026
See all related articles

This review explores epithelial drug transport in mucosal delivery, focusing on the intestinal dipeptide transporter PepT1. This transporter is key for targeting drugs to tumor cells, with less known about oral cavity drug absorption.

Area of Science:

  • Pharmacology
  • Cell Biology
  • Drug Delivery

Background:

  • Mucosal drug delivery involves epithelial transport, crucial for oral cavity and gastrointestinal tract absorption.
  • Cytotoxic chemotherapeutic drugs often cause side effects in these mucosae.
  • Carrier-mediated transport is a key mechanism in mucosal drug absorption.

Purpose of the Study:

  • To review epithelial drug transport mechanisms in mucosal drug delivery.
  • To highlight the role of the intestinal dipeptide transporter PepT1 in this process.
  • To compare drug transport in the gastrointestinal tract versus the oral cavity.

Main Methods:

  • Literature review focusing on carrier-mediated transport and PepT1.
  • Analysis of PepT1's presence and robustness in tumor epithelial cells.

Related Experiment Videos

  • Comparison of drug transport knowledge between gastrointestinal and buccal mucosae.
  • Main Results:

    • The intestinal dipeptide transporter PepT1 is enriched in tumor epithelial cells.
    • PepT1 is relatively resistant to cytotoxic chemotherapeutic drugs.
    • PepT1 shows potential for molecular engineering of targeted cancer drugs.
    • Drug transport in buccal epithelial cells is less understood than in the gastrointestinal tract.

    Conclusions:

    • PepT1 is a promising target for developing chemotherapeutic drugs with enhanced efficacy and reduced side effects.
    • Further research is needed to understand and optimize drug transport in the buccal mucosa for therapeutic applications.