Diagnosis is a fundamental stage in health care and medical treatment. Microfluidic biosensors and lab-on-a-chip devices are amongst the few practical tools for achieving this goal. A new computational code, specifically for designing microfluidic-integrated biosensors is developed, the details of which is presented in this work. This new approach is developed using control-volume based finite-element (CVFEM) method and solves bio-recognition chemical reactions and full Navier–Stokes equations. The results of the proposed platform are validated against the experimental data for a microfluidic based biosensor, where excellent agreement is achieved. The properties of the biosensor, sample, buffer fluid and even the microfluidic channel can easily be modified in this platform. This feature provides the scientific community with the ability to design a specific biosensor for requested point-of-care applications.•A new approach is developed using control-volume based finite-element (CVFEM) method for investigating flow inside a microfluidic-integrated biosensor. It is also used to study the influence of surface functionalization on binding cycle.•The proposed model solves bio-recognition chemical reactions as well as full Navier–Stokes and energy equations. Experimental-based or personalized equations of the chemical reactions and flow behaviour are adoptable to this code.•The developed model is Fortran-based and has the potential to be used in both industry and academia for biosensing technology.

Biosensors are favored devices for the fast and cost-effective detection of biological species without the need for laboratories. Microfluidic integration with biosensors has advanced their capabilities in selectivity, sensitivity, controllability, and conducting multiple binding assays simultaneously. Despite all the improvements, their design and fabrication are still challenging and time-consuming. The current study aims to enhance microfluidic-integrated biosensors’ performance. Three different functional designs are presented with both active (with the help of electroosmotic flow) and passive (geometry optimization) methods. For validation and further studies, these solutions are applied to an experimental setup for DNA hybridization. The numerical results for the original case have been validated with the experimental data from previous literature. Convection, diffusion, migration, and hybridization of DNA strands during the hybridization process have been simulated with finite element method (FEM) in 3D. Based on the results, increasing the velocity on top of the functionalized surface, by reducing the thickness of the microchamber in that area, would increase the speed of surface coverage by up to 62%. An active flow control with the help of electric field would increase this speed by 32%. In addition, other essential parameters in the fabrication of the microchamber, such as changes in pressure and bulk concentration, have been studied. The suggested designs are simple, applicable and cost-effective, and would not add extra challenges to the fabrication process. Overall, the effect of the geometry of the microchamber on the time and effectiveness of biosensors is inevitable. More studies on the geometry optimization of the microchamber and position of the electrodes using machine learning methods would be beneficial in future works.