Tumor-Organ-On-A-Chip Model Development Service

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Background Tumor-on-a-chip Applications Why Choose Us? FAQs Products

Are you currently facing challenges in accurately modeling the complex cochlear environment, experiencing limitations with traditional animal models, or struggling with the high costs and time associated with inner ear drug development? Creative Biolabs' Tumor-on-a-chip Model Development Service helps you overcome these hurdles and accelerate your research through cutting-edge microfluidic technology and advanced cell culture techniques. We provide you with a physiologically relevant and highly controllable in vitro platform for studying cochlear function, disease mechanisms, and therapeutic interventions.

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Background

Tumor diseases became the world's second-leading cause of mortality in 2018. Global data from 2020 indicates roughly 19.3 million incident cancer cases and 10 million deaths linked to oncological conditions. Extensive scientific investigations target the molecular drivers of tumor initiation, metastatic dissemination, and pathological progression. Traditional monolayer cell culture systems have prevailed in drug development research for generations, favored for low technical complexity and economic viability. These systems involve adherent cellular monolayers on non-compliant substrates, propagating within simplified nutrient conditions. While enabling basic cellular proliferation analyses, 2D configurations distort native cell morphology, cytoskeletal organization, and paracrine communication networks. Crucially, they lack the three-dimensional scaffolding essential for emulating histological complexity. This structural deficit prevents physiologically relevant extracellular matrix (ECM) engagement—known to regulate neoplastic behavior via mechanotransduction and biochemical signaling—rendering 2D platforms inadequate for replicating in vivo tumor microenvironments.

Fig 1. Schematic of the tumor microenvironment (TME). (OA Literature)Fig 1. The tumor microenvironment (TME).1,4

Tumor-on-a-chip

The tumor-on-chip platform demonstrates distinctive capabilities in vascular network development. This system integrates three-dimensional neoplastic constructs with precision-engineered fluidic architectures, maintaining continuous nutrient delivery while modeling biological transport phenomena including vascular dynamics and molecular exchange. Fabrication typically initiates with scaffold-based methodologies for 3D tumor analogs, subsequently integrated into microfluidic platforms. Advanced manufacturing approaches like soft lithographic patterning and additive bioprinting enables histologically relevant assemblies of malignant, stromal, and endothelial components. Core techniques encompass spheroid aggregation, bioink deposition, and scaffold templating.

Fig 2. Schematic of tumor-on-a-chip platforms. (OA Literature)Fig 2. Tumor-on-a-chip platforms.2,4

Microfluidic technology, emerging from the interdisciplinary convergence of cellular biology and microfabrication, maintains cellular viability within micron-scale microenvironments through picoliter-scale fluidic manipulation. Fluid dynamics are precisely orchestrated through engineered micro-conduits interfaced with microfluidic systems, enabling spatiotemporal regulation of tumor microenvironmental parameters to quantify cellular kinetics and live-cell transport phenomena. Device microarchitectures incorporate cell-laden hydrogels or perfusible lumen networks, emulating biomechanical forces and architectural constraints characteristic of living tissues. Diverse chip iterations now facilitate mechanistic investigations into neoplastic phenotypes, metastatic behavior, vascular morphogenesis, and therapeutic compound evaluation.

Fig 3. Vascularization in microfluidic chips. (OA Literature)Fig 3. Vascularization in microfluidic devices.3,4

Innovative microphysiological tumor platforms enable comprehensive investigation of oncological processes including proliferation, vascularization, metastatic behavior, and therapeutic response. By integrating precision biofabrication methods—such as photolithography, soft lithography, and 3D bioprinting—with microfluidic controls and tissue engineering principles, these systems recapitulate critical tumor microenvironment features: molecular gradient systems, dynamic cell-ECM interactions, and multicellular architectures incorporating malignant and stromal populations.

Table 1. Summary of the different types of tumor-on-a-chip.2,4

Tumor-on-a-chip models Cell types Applications
Lung tumor chip Human NSCLC cell line Explain the high level of resistance to therapy in lung cancer patients and provide an experimental model to study cancer persister cells and mechanisms of tumor dormancy in vitro
Human alveolar epithelial cells and human pulmonary microvascular endothelial cells Reconstitute the critical functional alveolar-capillary interface of the human lung to respond to bacteria and inflammatory cytokines introduced into the alveolar space
Brain tumor chip Brain tumor stem‐like cells Examine the function of primary patient‐derived BTSCs
Glioblastoma cells (U87) Develop a 3D brain cancer chip for drug screening
C6 glioma cells Study the cellular response to different concentrations of colchicines
Liver tumor chip HepG2/C3A
MEG‐01
MES‐SA
MES‐SA/DX‐5
Provide a combined strategy for selectively inhibiting MES‐SA/DX‐5 cell proliferation; may prove to be advantageous in vivo by specifically targeting MDR cancer with acceptable side effects
iPS C2a
Functional endothelial cells
Cardiomyocytes hepatocytes
Refine microtissues, establish modular multi-tissue platforms, and study interactive responses of cardiac, vascular, and hepatic microtissues to pharmacological agents and physiological and pathological stimuli
Colorectal-tumor chip CRC cell line HCT-116 Evaluate precision nanomedicine delivery
Breast tumor chip MDA-MB-453, MDA-MB-231, and HCC1937 Develop a microfluidic device for a 3D breast cancer screening platform
Pancreatic tumor chip MIA PaCa-2
BxPC3
HT-29
Replicate cellular morphologies and reflect the death of endothelial cells during the metastasis process
HepG2s
MSCs
HUVECs
Provide a suitable platform for pancreatic cancer cell growth for studying the metastasis of pancreatic cancer

Applications

Creative Biolabs' Tumor-On-A-Chip Model Development Service can be applied to a wide range of cancer research applications, including:

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Why Choose Us?

Creative Biolabs is a trusted partner for researchers and biopharmaceutical companies seeking advanced in vitro models for cancer research. Our Tumor-On-A-Chip Model Development Service offers several key advantages:

FAQs

Q: What types of tumor models can Creative Biolabs develop?
A: Creative Biolabs can develop a wide range of customized tumor-on-a-chip models, including models of solid tumors, metastatic tumors, and specific cancer types such as breast cancer, lung cancer, and colorectal cancer. We can incorporate various cell types, ECM components, and microenvironmental factors to meet your specific research needs. Contact us to discuss your specific model requirements.
Q: How do microfluidic tumor models outperform conventional cultures?
A: Microfluidic tumor platforms demonstrate enhanced biomimetic fidelity through precise microenvironmental modulation, reduced preclinical animal reliance, and increased therapeutic response predictability. These systems achieve superior pathophysiological recapitulation of living tumor ecosystems, yielding results with higher clinical translatability than conventional methodologies.
Q: Is it possible to develop a tumor-on-a-chip model for my specific research needs, even if it's highly specialized?
A: Absolutely! Creative Biolabs specializes in developing customized solutions. We encourage you to contact our team to discuss your unique research requirements. We will work closely with you to design and develop a Tumor-on-a-chip model that meets your exact specifications.

Recommended Products

For researchers facing challenges in initiating microfluidic cellular investigations de novo, Creative Biolabs' engineered cell-culture systems deliver integrated solutions that streamline workflow bottlenecks.

Distributed under Unsplash License, from Unsplash.

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.

MFMM1-GJS3 BE-Transflow Standard Construction of ALI interface and for organ chips such as lung, skin, intestine, cornea, etc.

MFMM1-GJS4 BE-Doubleflow Standard Best choice for studying circulating particles, cell interactions, and simple organ-on-chip system construction.

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

MFCH-009 Synvivo-Idealized Co-Culture Network Chips (IMN2 Radial) 3D Blood Brain Barrier Model
3D Inflammation Model
3D Cancer Model
3D Toxicology Model

MFCH-010 Synvivo-Idealized Co-Culture Network Chips (IMN2 TEER) 3D Blood Brain Barrier Model
3D Inflammation Model
3D Cancer Model
3D Toxicology Model

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

MFCH-012 Synvivo-SMN2 microvascular network Co-Culture Chips 3D Inflammation Model
3D Cancer Model
3D Toxicology Model
3D Lung Model

For more information about Creative Biolabs products and services, please contact us.

References

  1. Ahn, Jungho, et al. "Tumor microenvironment on a chip: the progress and future perspective." Bioengineering 4.3 (2017): 64.
  2. Liu, Xingxing, et al. "Tumor-on-a-chip: from bioinspired design to biomedical application." Microsystems & Nanoengineering 7.1 (2021): 50.
  3. Wang, Ruixin, et al. "Tumor-on-a-chip: Perfusable vascular incorporation brings new approach to tumor metastasis research and drug development." Frontiers in Bioengineering and Biotechnology 10 (2022): 1057913.
  4. Distributed under Open Access license CC BY 4.0, without modification.

For Research Use Only. Not For Clinical Use.

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