Table 1.
Classification | Merits and demerits | Biomaterials | Applications | Ref. |
---|---|---|---|---|
Synthetic polymers | Inexpensive and can be manipulated easily; tunable mechanical properties and high malleability; lack of or limited biocompatibility Foreign body response; adverse immunologic reactions; lack of adhesion to living tissues |
PLA | Combined with autologous chondrocytes to construct penile prostheses | [22] |
PGA | Combined with cells to reconstruct the smooth muscle tissue of the cavernous body | [23] | ||
PDMS | Coculture of embryonic stem cells and testicular cells; Microfluidic devices | [26,90] | ||
PLGA | In vitro spermatogenesis of immature spermatogenic germ cells | [27] | ||
PEG |
3D follicular culture |
[92] |
||
Natural polymers (hydrogels) | High-water content; excellent biodegradability and biocompatibility; environmental stresses similar to tissue; can be easily loaded with other factors; maintain the 3D culture environment; ensure the effect of cell–cell interactions; Insufficient mechanical strength |
Hyaluronan-based hydrogels | In vitro maturation of follicles | [29] |
Gelatin-based hydrogel | Constructing placental barrier models | [31] | ||
Soft agar hydrogel | Coculture of spermatogonia and somatic cells | [81] | ||
Alginate-based hydrogels | In vitro follicular culture; in vivo transplantation of isolated preantral follicles and ovarian cells; 3D culture system for testicular cells | [32,54] | ||
Fibrin hydrogels; fibrin-alginate hydrogels; fibrin-collagen composites | Primordial follicle transplantation | [57,58] | ||
Collagen-based hydrogel | In vitro oocyte maturation of ovary follicles | [51] | ||
Matrigels |
Generation of functional spermatids from human SSCs in vitro; testicular, ovarian, and endometrial organoids |
[[40], [41], [42], [43], [44], [45],55] |
||
Natural polymers (scaffolds) | Porous structure, good tissue integration; can be loaded with cell growth factors and drugs; improve angiogenesis Insufficient mechanical strength |
Collagen scaffolds | Loaded with human umbilical cord-derived mesenchymal stem cells/bone marrow mesenchymal stem cells for endometrial regeneration | [28,117] |
Alginate-based macroporous scaffolds | Culture and growth of primitive follicles | [126] | ||
Gelatin-based scaffolds |
Create a bioprosthetic ovary; endometrial repair; functional reconstruction of injured corpus cavernosa |
[30,59,119] |
||
Acellular matrices | Retention of the bioactive matrix; Structural integrity with better mechanical performance Need improvements in terms of the morphology and precise structure of the original tissue after decellularization; cell filling rate during the recellularization process needs to be improved |
Acellular porcine small intestinal submucosa graft | Cervicovaginal reconstruction | [127] |
Corpora collagen matrices | Functional restoration of the penis | [62,66] | ||
Autologous cartilage rods | Penile prostheses | [67] | ||
Amniotic membrane | Penile reconstruction (treatment of Peyronie's disease) | [128] | ||
Acellular uterus | Recellularized in vitro with primary uterine cells (Bioengineered uterine tissue) | [[68], [69], [70], [71]] | ||
Bovine pericardium | Potential scaffold for testicular repair | [72] | ||
Ovarian scaffolds | Artificial ovaries | [63,64] | ||
Decellularized placental scaffold | 3D dynamic culture of mouse embryonic fibroblasts | [70] | ||
Acellular testis | Testicular organoid construction | [[73], [74], [75]] |