Tunable degradation in hydrogel microparticles
Non-alginate hydrogel microparticles for localized delivery and sustained release of therapeutic cells and/or tissues (including homogenous or heterogenous cell clusters) at a site of implantation. The microparticles comprise a 3-dimensional matrix of covalently crosslinked non-alginate polymer compounds and a therapeutically-effective amount of cells and/or tissue entrapped therein, wherein the cells have a viability of at least about 50%, and wherein the microparticle has a size of greater than about 30 pm. Compositions containing such microparticles and methods of using such microparticles for treatment are also described.
1 . A method for localized delivery and sustained release of therapeutic cells and/or tissues at a site of implantation, said method comprising administering a plurality of spherical or ellipsoidal microparticles to a site of implantation in a subject, wherein each microparticle in said plurality of microparticles is a non-alginate hydrogel microparticle comprising a 3-dimensional matrix of covalently crosslinked non-alginate polymer compounds and a therapeutically-effective amount of cells and/or tissue entrapped therein, wherein said cells have a viability of at least about 50%, and wherein each of said microparticles has a size of greater than about 30 μm, and wherein each of said microparticles is formed without oil-emulsion, and wherein said non-alginate polymer compounds are polyethylene glycol maleimide, polyethylene glycol vinyl sulfone, or acrylated hyaluronic acid, said matrix further comprises crosslinking agents crosslinked with said non-alginate polymer compounds selected from the group consisting of dithiothreitol, polyethylene glycol dithiol, ethylene glycol bis-mercaptoacetate, and combinations thereof.
2 . The method of claim 1 , wherein said microparticles biodegrade within about 3 months after said administration.
3 . The method of claim 1 , wherein said microparticles do not biodegrade for at least 6 months after said administration.
4 . The method of claim 1 , wherein said hydrogel microparticles adhere to tissue at the site of implantation thereby maintaining the implanted cells at the site of implantation for a therapeutic amount of time.
5 . The method of claim 1 , wherein said 3-dimensional matrix consists essentially of covalently crosslinked polyethylene glycol maleimide and polyethylene glycol dithiol precursor compounds.
6 . The method of claim 1 , wherein said 3-dimensional matrix consists essentially of covalently crosslinked polyethylene glycol vinyl sulfone and dithiothreitol or ethylene glycol bis-mercaptoacetate precursor compounds.
7 . The method of claim 1 , wherein up to 50% of the volume of said microparticle comprises said cells or tissue.
8 . The method of claim 1 , wherein said microparticle has storage stability in PBS at 37° C. of less than 6 months.
9 . The method of claim 1 , wherein said microparticle has storage stability in PBS at 37° C. of greater than 6 months.
10 . The method of claim 1 , wherein said microparticle is a degradable microparticle that will break down in less than 3 months when implanted in vivo.
11 . The method of claim 1 , wherein said microparticle is a durable microparticle that will not break down for at least 3 months when implanted in vivo.
12 . The method of claim 1 , further comprising cell media components.
13 . The method of claim 1 , wherein said cells are non-proliferative or proliferative.
14 . The method of claim 1 , further comprising cellular products secreted along with the cells include signaling molecules, cytokines, chemokines, therapeutic proteins, hormones, vesicles, antibodies, viruses, exosomes, and the like.
15 . The method of claim 1 , wherein said cells are engineered or transgenic cells.
16 . The method of claim 1 , wherein said cells are clusters of a plurality of aggregated cells.
17 . The method of claim 16 , wherein said clusters comprise two or more different types of cells.
18 . The method of claim 1 , wherein said microparticle has a size of from about 50 μm to about 5 mm.
19 . The method of claim 1 , said method comprising administering a composition comprising a plurality of said hydrogel microparticles dispersed or suspended in a biocompatible delivery vehicle to said site of implantation in said subject.