Related Experiment Video
Updated: Apr 7, 2026

FtsZ Polymerization Assays: Simple Protocols and Considerations
Published on: November 16, 2013
Mechanism of Hydrolytic Instability of ZIF‑8 in Aqueous and Buffered Media: Implications on Drug Delivery
Eman Wahid1, Worood A El-Mehalmey1, Asmaa Naser2
1Center for Material Science, Zewail City of Science and Technology, Giza 12578, Egypt.
Abstract:
Despite widespread assumptions of ZIF-8 stability in aqueous media, we demonstrate that the apparent endurance of ZIF-8 is largely misconceived as thermodynamic stability rather than correctly ascribed as kinetic stability under a certain experimental setup. In unbuffered solutions, the rapid release of zinc and 2-methylimidazole ligands causes an instantaneous pH spike, which inhibits further degradation. This self-protective mechanism is, however, nullified in buffered environments, where ZIF-8 undergoes a rapid and spontaneous decomposition. Our findings ascertain a critical thermodynamic instability of ZIF-8 under physiologically relevant conditions. The findings of this investigation necessitate a fundamental re-evaluation of ZIF-8 suitability for water-based applications, particularly drug delivery. Furthermore, the insights and methodology presented herein provide a crucial framework for predicting the stability of similar metal-organic frameworks in aqueous solutions under biologically relevant conditions.
Related Concept Videos
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
Amides to Carboxylic Acids: Hydrolysis
Acid-catalyzed hydrolysis:
Hydrolysis of amides under acidic conditions yields carboxylic acids. Since the reaction occurs slowly, hydrolysis requires the conditions of heat.
The mechanism begins with the protonation of the carbonyl oxygen by the acid catalyst. The protonation makes the amide carbonyl carbon more...
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Hydrolysis
Hydrolysis is a chemical reaction in which the addition of water breaks down a polymer into its simpler monomer units. For example, peptides break into amino acids, carbohydrates into simple sugars, and DNA into nucleotides. Enzymes often facilitate these processes.
Hydrolysis Reverses Dehydration Synthesis
Complex carbohydrates can be broken down by breaking the bonds between individual sugar units. The reaction breaks a glycosidic bond as water is added to the compound. The...
Destabilization of Microtubules
Weak Acid Solutions

