Multifunctional nanoplatforms co-delivering combinatorial dual-drug for eliminating cancer multidrug resistance

Theranostics. 2021 Apr 19;11(13):6334-6354. doi: 10.7150/thno.59342. eCollection 2021.

Abstract

Clinically, the primary cause of chemotherapy failure belongs to the occurrence of cancer multidrug resistance (MDR), which directly leads to the recurrence and metastasis of cancer along with high mortality. More and more attention has been paid to multifunctional nanoplatform-based dual-therapeutic combination to eliminate resistant cancers. In addition to helping both cargoes improve hydrophobicity and pharmacokinetic properties, increase bioavailability, release on demand and enhance therapeutic efficacy with low toxic effects, these smart co-delivery nanocarriers can even overcome drug resistance. Here, this review will not only present different types of co-delivery nanocarriers, but also summarize targeted and stimuli-responsive combination nanomedicines. Furthermore, we will focus on the recent progress in the co-delivery of dual-drug using such intelligent nanocarriers for surmounting cancer MDR. Whereas it remains to be seriously considered that there are some knotty issues in the fight against MDR of cancers via using co-delivery nanoplatforms, including limited intratumoral retention, the possible changes of combinatorial ratio under complex biological environments, drug release sequence from the nanocarriers, and subsequent free-drug resistance after detachment from the nanocarriers. It is hoped that, with the advantage of continuously developing nanomaterials, two personalized therapeutic agents in combination can be better exploited to achieve the goal of cooperatively combating cancer MDR, thus advancing the time to clinical transformation.

Keywords: cancer therapy; co-delivery; dual-drug; multidrug resistance; multifunctional nanoplatform.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B / antagonists & inhibitors
  • ATP-Binding Cassette Transporters / antagonists & inhibitors
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Apoptosis / drug effects
  • Doxorubicin / administration & dosage
  • Drug Carriers / administration & dosage*
  • Drug Carriers / pharmacokinetics
  • Drug Delivery Systems*
  • Drug Liberation
  • Drug Resistance, Multiple / drug effects*
  • Drug Resistance, Neoplasm / drug effects*
  • Gases / administration & dosage
  • Humans
  • Hydrogen-Ion Concentration
  • Nanostructures / administration & dosage*
  • Neoplasm Proteins / antagonists & inhibitors
  • Oxidation-Reduction
  • Peptides / administration & dosage
  • RNA, Small Interfering / administration & dosage
  • Surface-Active Agents / administration & dosage
  • Surface-Active Agents / therapeutic use
  • Theranostic Nanomedicine / methods*

Substances

  • ATP Binding Cassette Transporter, Subfamily B
  • ATP-Binding Cassette Transporters
  • Drug Carriers
  • Gases
  • Neoplasm Proteins
  • Peptides
  • RNA, Small Interfering
  • Surface-Active Agents
  • Doxorubicin