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. 2021 Mar 13;11(8):2362–2395. doi: 10.1016/j.apsb.2021.03.019

Table 5.

Current challenges and potential suggestions for MOFs-based DDS.

Challenge Suggestion
In vivo fates of MOFs and drugs loaded inside are unclear
  • • Choosing the appropriate animal model as preclinical evaluation

  • • Optimizing the preparations and administration routes

Current researches are limited to qualitative evaluation of MOFs
  • • Paying attention to quantitative quality control strategies for contents of MOFs

  • • Limiting starting materials for impurities control

Some MOFs are unstable in physiological conditions
  • • Surface functionalization of MOFs

  • • Combination with other more stable materials

Lack of systematic biosafety evaluation to MOFs
  • • Selecting metal ions and organic linkers with favorable biocompatibility

  • • Highlighting the pharmacokinetics mechanism as the whole ADME process

No established standard for MOFs classification and nomenclature
  • • Unifying the naming rules of MOFs