Translational Nanomedicines Across Human Reproductive Organs Modeling on Microfluidic Chips: State-of-the-Art and Future Prospects

Ankur Sood, Anuj Kumar, Vijai Kumar Gupta, Chul Min Kim, Sung Soo Han*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

6 Citations (Scopus)
3 Downloads (Pure)


Forecasting the consequence of nanoparticles (NPs) and therapeutically significant molecules before materializing for human clinical trials is a mainstay for drug delivery and screening processes. One of the noteworthy obstacles that has prevented the clinical translation of NP-based drug delivery systems and novel drugs is the lack of effective preclinical platforms. As a revolutionary technology, the organ-on-a-chip (OOC), a coalition of microfluidics and tissue engineering, has surfaced as an alternative to orthodox screening platforms. OOC technology recapitulates the structural and physiological features of human organs along with intercommunications between tissues on a chip. The current review discusses the concept of microfluidics and confers cutting-edge fabrication processes for chip designing. We also outlined the advantages of microfluidics in analyzing NPs in terms of characterization, transport, and degradation in biological systems. The review further elaborates the scope and research on translational nanomedicines in human reproductive organs (testis, placenta, uterus, and menstrual cycle) by taking the advantages offered by microfluidics and shedding light on their potential future implications. Finally, we accentuate the existing challenges for clinical translation and scale-up dynamics for microfluidics chips and emphasize its future perspectives.

Original languageEnglish
Pages (from-to)62-84
JournalACS Biomaterials Science and Engineering
Issue number1
Early online date21 Dec 2022
Publication statusPrint publication - 9 Jan 2023

Bibliographical note

Publisher Copyright:
© 2022 American Chemical Society.


  • biosensing
  • drug delivery
  • microfluidics
  • nanomedicine
  • organ-on-a-chip
  • preclinical assessment
  • Nanoparticles
  • Microphysiological Systems
  • Humans
  • Nanomedicine
  • Microfluidics
  • Tissue Engineering


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