Are you currently facing challenges in studying ovarian follicle development, reproductive toxicology, or developing new fertility preservation strategies? Creative Biolabs' Ovary-On-A-Chip Model Development Service offers a comprehensive solution for researchers seeking to advance their studies of ovarian function and related reproductive processes. We provide customized microfluidic devices that replicate the intricate three-dimensional structure and dynamic flow conditions of the native ovary, enabling more physiologically relevant in vitro studies.
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The paired ovarian organs, positioned bilaterally flanking the uterus and linked via the uterine tubes, serve dual physiological roles in female reproduction. Their primary role involves gamete production—from puberty onward, these glands contain numerous follicular units housing immature ova. Simultaneously, ovarian endocrine activity regulates systemic physiology through steroid hormone synthesis (estrogens, progestogens, androgens) and growth mediator secretion. These biomolecules orchestrate multisystem functions spanning skeletal integrity, immunomodulation, neural signaling, and reproductive cyclicity while sustaining menstrual rhythm.
Fig 1. Ovaries and ovarian organ-on-a-chip.1,3
Currently, murine models remain the sole species achieving complete follicular development from primordial stages to live births via assisted reproduction. While pivotal for decoding conserved folliculogenesis mechanisms, translation to humans or livestock falters due to two biological constraints: extended maturation timelines and significant volumetric scaling. Consequently, effective in vitro systems for larger mammals require dynamic culture platforms that accommodate prolonged developmental phases and substantial structural expansion.
Organ-on-a-chip (OOC) platforms emulate living systems through biomimetic tissue architectures that maintain inter-organ communication while sustaining critical biological functions. These microphysiological systems surpass conventional preclinical approaches (static cultures and animal testing) through enhanced physiological accuracy, experimental reproducibility, and multi-tissue integration capabilities. Their modular design enables precise control over tissue-specific parameters, standardized culture conditions, and cost-effective scalability—advantages accelerating adoption across pharmacological screening and mechanistic pathophysiological investigations. This technological paradigm shift promises transformative impacts on therapeutic development and biomedical discovery.
Ex vivo ovarian culture systems offer critical pathophysiological insights for reproductive biology and significant fertility preservation applications. This microfluidic-based platform integrates lab-grown follicular organoids with dynamic culture arrays. Ovarian units across species and developmental phases—including preantral, antral, and cumulus-oocyte complexes—are encapsulated within biomimetic matrices (variable-stiffness core-shell capsules, alginate hydrogels, or cortical tissue scaffolds) to replicate native ovarian microenvironments. Such engineered models advance mechanistic understanding of folliculogenesis while enabling systematic analysis of developmental modulators and ovulation triggers.
The ovulatory cycle orchestrates intricate endocrine signaling across organs through precise spatiotemporal coordination, directing either embryogenesis initiation or cyclical endometrial renewal. Complementing miniaturized automation, organ-chip technology employs high-precision flow modulation to regulate biomolecular gradients. Leveraging this, scientists engineered a murine follicular interface generating human 28-day hormonal rhythms, synchronizing reproductive tract dynamics across modular units—single, dual, and multi-tissue configurations (Solo-MFP, Duet-MFP, Quintet-MPF).
Fig 2. Microfluidic platform supported follicle maturation and hormone secretion in the Solo-MFP.2,3
The Quintet-MPF platform incorporates five primary cellular modules (cervical, fallopian, murine ovarian, uterine, and hepatic tissues) into an integrated biochip system termed "EVATAR." Through controlled gonadotropin stimulation, ovarian components generate steroid and peptide hormones that interact dynamically with downstream reproductive tissues and hepatic counterparts. This multi-organ architecture enables novel applications in pharmacological innovation—from fertility modulation therapies to compound toxicity evaluation—by recapitulating systemic hormone-mediated responses.
Current investigations into ovarian epithelial cells' endocrine regulatory mechanisms remain incomplete, requiring urgent methodological refinement. Future studies will prioritize ultraprecise systems that synchronize with cyclical physiological oscillations. Innovations in ovarian pathophysiological platforms—such as vascular network engineering, biomechanical force emulation, and multi-tissue microphysiological integration—represent a transformative paradigm for addressing clinical subfertility.
Ovary-on-a-chip models have a wide range of applications in reproductive biology research and related fields. These include:
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Creative Biolabs' Ovary-On-A-Chip Model Development Service offers several key advantages:
Here are some frequently asked questions from potential customers interested in our Ovary-On-A-Chip Model Development Service:
For researchers facing challenges in initiating microfluidic cellular investigations de novo, Creative Biolabs' engineered cell-culture systems deliver integrated solutions that streamline workflow bottlenecks.
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CBLcell™ Organ-on-chip Cell Culture Platform
Creative Biolabs provides you with a full range of microfluidic organ-on-a-chip and cell culture instruments and services to facilitate the start of your research to the greatest extent. If you are overwhelmed by starting a microfluidic cell experiment from scratch, Creative Biolabs' customized platform for cell culture can perfectly solve your problem.
Our chips offer the freedom to choose the cell seeding channels and perfusion conditions, enabling various cell culture modes.
CAT | Product Name | Application | Figure |
MFMM1-GJS1 | BE-Flow Standard | 2D/3D cell culture and mechanical shear stress studies by means of microfluidics. |
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MFMM1-GJS3 | BE-Transflow Standard | Construction of ALI interface and for organ chips such as lung, skin, intestine, cornea, etc. |
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MFMM1-GJS4 | BE-Doubleflow Standard | Best choice for studying circulating particles, cell interactions, and simple organ-on-chip system construction. |
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MFMM-0723-JS1 | Synvivo-SMN1 Microvascular Network Chips |
Flow research Shear stress effect Vascular disease research Drug delivery Drug discovery Cellular behavior Cell-cell/particle interaction |
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MFCH-009 | Synvivo-Idealized Co-Culture Network Chips (IMN2 Radial) |
3D Blood Brain Barrier Model 3D Inflammation Model 3D Cancer Model 3D Toxicology Model |
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MFCH-010 | Synvivo-Idealized Co-Culture Network Chips (IMN2 TEER) |
3D Blood Brain Barrier Model 3D Inflammation Model 3D Cancer Model 3D Toxicology Model |
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MFCH-011 | Synvivo-Idealized Co-Culture Network Chips (IMN2 Linear) |
3D Blood Brain Barrier Model 3D Inflammation Model 3D Cancer Model 3D Toxicology Model 3D Lung Model 3D ALI Chip |
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MFCH-012 | Synvivo-SMN2 microvascular network Co-Culture Chips |
3D Inflammation Model 3D Cancer Model 3D Toxicology Model 3D Lung Model |
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References
For Research Use Only. Not For Clinical Use.