A nanodroplet cell processing platform facilitating drug synergy evaluations for anti-cancer treatments

Therapeutic drug synergism intervened in cancer treatments has been demonstrated to be more effective than using a single effector. However, it remains inherently challenging, with a limited cell count from tumor samples, to achieve potent personalized drug cocktails. To address the issue above, we herein present a nanodroplet cell processing platform. The platform incorporates an automatic nanodroplet dispenser with cell array ParaStamp chips, which were fabricated by a new wax stamping approach derived from laser direct writing. Such approach enables not only the on-demand de-wetting with hydrophobic wax films on substrates but also the mask-less fabrication of non-planar microstructures (i.e. no photolithography process). The ParaStamp chip was pre-occupied with anti-cancer drugs and their associate mixtures, enabling for the spatially addressable screening of optimal drug combinations simultaneously. Each droplet with a critical volume of 200 nl containing with 100 cells was utilized. Results revealed that the optimal combination reduces approximate 28-folds of conducted doses compared with single drugs. Tumor inhibition with the optimally selected drug combination was further confirmed by using PC-3 tumor-bearing mouse models. Together, the nanodroplet cell processing platform could therefore offer new opportunities to power the personalized cancer medicine at early-stage drug screening and discovery.

[1]  D. Troyer,et al.  Genetic determinants of response to chemotherapy in transgenic mouse mammary and salivary tumors , 2000, Oncogene.

[2]  M. Ferrer,et al.  Quantitative high throughput screening using a primary human three-dimensional organotypic culture predicts in vivo efficacy , 2015, Nature Communications.

[3]  Yiling Lu,et al.  Identification of optimal drug combinations targeting cellular networks: integrating phospho-proteomics and computational network analysis. , 2010, Cancer research.

[4]  Chang-Yu Chen,et al.  Patch clamping on plane glass-fabrication of hourglass aperture and high-yield ion channel recording. , 2009, Lab on a chip.

[5]  Chen-Ho Wang,et al.  Dielectrophoresis-based cellular microarray chip for anticancer drug screening in perfusion microenvironments. , 2011, Lab on a chip.

[6]  Chih-Ming Ho,et al.  Output-driven feedback system control platform optimizes combinatorial therapy of tuberculosis using a macrophage cell culture model , 2016, Proceedings of the National Academy of Sciences.

[7]  William R. Sones,et al.  Haemotoxicity of busulphan, doxorubicin, cisplatin and cyclophosphamide in the female BALB/c mouse using a brief regimen of drug administration , 2011, Cell Biology and Toxicology.

[8]  Eric Schmitt,et al.  Droplet-microarray on superhydrophobic–superhydrophilic patterns for high-throughput live cell screenings , 2016 .

[9]  Douglas A Lauffenburger,et al.  Addressing genetic tumor heterogeneity through computationally predictive combination therapy. , 2013, Cancer discovery.

[10]  Chang-Yu Chen,et al.  Separation and detection of rare cells in a microfluidic disk via negative selection. , 2011, Lab on a chip.

[11]  R. Sun,et al.  Closed-loop control of cellular functions using combinatory drugs guided by a stochastic search algorithm , 2008, Proceedings of the National Academy of Sciences.

[12]  Ming-Chih Ho,et al.  A planar interdigitated ring electrode array via dielectrophoresis for uniform patterning of cells. , 2008, Biosensors & bioelectronics.

[13]  Utkan Demirci,et al.  Rapid Assembly of Heterogeneous 3D Cell Microenvironments in a Microgel Array , 2016, Advanced materials.

[14]  Benjamin P. C. Chen,et al.  ParaStamp and Its Applications to Cell Patterning, Drug Synergy Screening, and Rewritable Devices for Droplet Storage , 2017, Advanced Biosystems.

[15]  Yusuke Hara,et al.  A simple method for producing multiple copies of controlled release small molecule microarrays for cell-based screening , 2016, Biofabrication.

[16]  G. Bonadonna,et al.  Combination chemotherapy as an adjuvant treatment in operable breast cancer. , 1976, The New England journal of medicine.

[17]  Ming-Rong Zhang,et al.  High-throughput screening with nanoimprinting 3D culture for efficient drug development by mimicking the tumor environment. , 2015, Biomaterials.

[18]  M. Yen,et al.  A transparent cell-culture microchamber with a variably controlled concentration gradient generator and flow field rectifier. , 2008, Biomicrofluidics.

[19]  Pascal Colpo,et al.  Multiplex cell microarrays for high-throughput screening. , 2016, Lab on a chip.

[20]  Yang Zeng,et al.  Biomechanically primed liver microtumor array as a high-throughput mechanopharmacological screening platform for stroma-reprogrammed combinatorial therapy. , 2017, Biomaterials.

[21]  C. Long,et al.  Taxol arrests the development of blood-stage Plasmodium falciparum in vitro and Plasmodium chabaudi adami in malaria-infected mice. , 1994, The Journal of clinical investigation.

[22]  Chih-Ming Ho,et al.  A streamlined search technology for identification of synergistic drug combinations , 2015, Scientific Reports.

[23]  C. Miller,et al.  Vinorelbine tartrate and paclitaxel combinations: enhanced activity against in vivo P388 murine leukemia cells. , 1995, Journal of the National Cancer Institute.

[24]  Chiun-Sheng Huang,et al.  A Novel 96well-formatted Micro-gap Plate Enabling Drug Response Profiling on Primary Tumour Samples , 2015, Scientific Reports.

[25]  P. Levkin,et al.  Droplet‐Array (DA) Sandwich Chip: A Versatile Platform for High‐Throughput Cell Screening Based on Superhydrophobic–Superhydrophilic Micropatterning , 2015, Advanced materials.

[26]  E. Scott,et al.  Drug-eluting microarrays to identify effective chemotherapeutic combinations targeting patient-derived cancer stem cells , 2015, Proceedings of the National Academy of Sciences.

[27]  V. Budach,et al.  Efficacy of ifosfamide, dacarbazine, doxorubicin and cisplatin in human sarcoma xenografts. , 1994, British Journal of Cancer.

[28]  Cheng-Wey Wei,et al.  Direct-write laser micromachining and universal surface modification of PMMA for device development , 2004 .

[29]  Susan E. Abbatiello,et al.  Erratum: Synergistic drug combinations tend to improve therapeutically relevant selectivity , 2009, Nature Biotechnology.

[30]  G. Hortobagyi,et al.  Long-term follow-up of patients with complete remission following combination chemotherapy for metastatic breast cancer. , 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[31]  Chih-Ming Ho,et al.  Rapid optimization of drug combinations for the optimal angiostatic treatment of cancer , 2015, Angiogenesis.