This paper investigates
self-sorting and triggered assembly of
multicomponent gels that combine sorbitol-based low-molecular-weight
gelator (LMWG) DBS-CONHNH2 and peptide-based LMWG Nap-FF,
with the assembly of Nap-FF being triggered either using glucono-δ-lactone
(GdL) to lower pH or CaCl2. Changing triggers alters the
way Nap-FF assembles on the molecular scale either as its acid form
or its calcium salt, leading to different nanoscale networks and rheological
behaviors. The choice of trigger impacts the properties of the two-component
gels formed with DBS-CONHNH2. Using either trigger, the
LMWGs self-sort on the molecular level into their own distinct assemblies.
However, when using a GdL trigger, the sheet-like Nap-FF assemblies
encourage DBS-CONHNH2 assembly, with the two assemblies
interacting with one another on a network level as a result of interactions
between the acylhydrazide and the carboxylic acid. Conversely, when
using a CaCl2 trigger, the two fibrillar assemblies are
independent of one another on the network level, with the carboxylic
acid being bound to calcium in the form of its carboxylate salt, and
unable to interact with DBS-CONHNH2. As such, GdL-triggering
leads to molecular-level self-sorting and network-level coassembly,
while CaCl2-triggering leads to both molecular-level and
network-level self-sorting. Injecting the CaCl2 trigger
into a preformed DBS-CONHNH2 gel, followed by its diffusion,
creates dynamic, evolving, spatially-resolved self-sorted multicomponent
gels, with stiffnesses differing by 2 orders of magnitude in different
domains. Given the mild, biocompatible nature of CaCl2,
it is suggested that this calcium ion diffusion approach to spatiotemporally
resolved patterning of multidomain gels may have future relevance
in cell-based studies.