Enteral Route Nanomedicine for Cancer Therapy

Int J Nanomedicine. 2024 Sep 25:19:9889-9919. doi: 10.2147/IJN.S482329. eCollection 2024.

Abstract

With the in-depth knowledge of the pathological and physiological characteristics of the intestinal barrier-portal vein/intestinal lymphatic vessels-systemic circulation axis, oral targeted drug delivery is frequently being renewed. With many advantages, such as high safety, convenient administration, and good patient compliance, many researchers have begun to explore targeted drug delivery from intravenous injections to oral administration. Over the past few decades, the fields of materials science and nanomedicine have produced various drug delivery platforms that hold great potential in overcoming the multiple barriers associated with oral drug delivery. However, the oral transport of particles into the systemic circulation is extremely difficult due to immune rejection and biochemical invasion in the intestine, which limits absorption and entry into the bloodstream. The feasibility of the oral delivery of targeted drugs to sites outside the gastrointestinal tract (GIT) is unknown. This article reviews the biological barriers to drug absorption, the in vivo fate and transport mechanisms of drug carriers, the theoretical basis for oral administration, and the impact of carrier structural evolution on oral administration to achieve this goal. Finally, this article reviews the characteristics of different nano-delivery systems that can enhance the bioavailability of oral therapeutics and highlights their applications in the efficient creation of oral anticancer nanomedicines.

Keywords: biological barriers; cancer treatment; nanoparticles; oral nanomedicine; oral targeted drug delivery.

Publication types

  • Review

MeSH terms

  • Administration, Oral
  • Animals
  • Antineoplastic Agents* / administration & dosage
  • Antineoplastic Agents* / chemistry
  • Antineoplastic Agents* / pharmacokinetics
  • Biological Availability
  • Drug Carriers / chemistry
  • Drug Delivery Systems / methods
  • Humans
  • Nanomedicine* / methods
  • Nanoparticles / administration & dosage
  • Nanoparticles / chemistry
  • Neoplasms* / drug therapy
  • Neoplasms* / therapy

Substances

  • Antineoplastic Agents
  • Drug Carriers

Grants and funding

This research was supported by the National Natural Science Foundation of China (82302330, 82372067, 82072039), Postdoctoral Fellowship Program of CPSF under Grant Number BX20230068, and Research Personnel Cultivation Program of Zhongda Hospital Southeast University (CZXM-GSP-RC81).