| Summary: | This contribution is aimed at extending our previous findings on the formation and stability of chitosan/hyaluronan-based complex coacervates. Colloids are herewith formed by harnessing electrostatic interactions between the two polyelectrolytes. The presence of tiny amounts of the multivalent anion tripolyphosphate (TPP) in the protocol synthesis serves as an adjuvant “point-like” cross-linker for chitosan. Hydrochloride chitosans at different viscosity average molar mass, <inline-formula> <math display="inline"> <semantics> <mrow> <mover accent="true"> <mrow> <msub> <mi>M</mi> <mi>v</mi> </msub> </mrow> <mo stretchy="true">¯</mo> </mover> </mrow> </semantics> </math> </inline-formula>, in the range 10,000−400,000 g/mol, and fraction of acetylated units, F<sub>A</sub>, (0.16, 0.46 and 0.63) were selected to fabricate a large library of formulations. Concepts such as coacervate size, surface charge and homogeneity in relation to chitosan variables are herein disclosed. The stability of coacervates in Phosphate Buffered Saline (PBS) was verified by means of scattering techniques, i.e., Dynamic Light Scattering (DLS) and Small-Angle X-ray Scattering (SAXS). The conclusions from this set of experiments are the following: (<i>i</i>) a subtle equilibrium between chitosan F<sub>A</sub> and <inline-formula> <math display="inline"> <semantics> <mrow> <mover accent="true"> <mrow> <msub> <mi>M</mi> <mi>v</mi> </msub> </mrow> <mo stretchy="true">¯</mo> </mover> </mrow> </semantics> </math> </inline-formula> does exist in ensuring colloidal stability; (<i>ii</i>) once diluted in PBS, osmotic swelling-driven forces trigger the enlargement of the polymeric mesh with an ensuing increase of coacervate size and porosity.
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