Immobilised Enzymes TRIZ Cases

A composite hydrophobic polymer shell improves microcapsule impermeability and keeps hydrophobic cores intact during high-temperature fiber spinning.

A solidifying phase-change matrix anchors rare cells during staining and washing, improving retention for single-cell analysis and diagnosis.

Solidifying a phase-change material immobilizes rare cells before staining, limiting wash-off and supporting precise single-cell analysis.

By immobilizing malodorous microorganisms on an evaporator surface, this case enables faster, field-like evaluation of vehicle AC odor reduction.

Multiple dispensing and inspection stations build tissue constructs in parallel to raise throughput, cut clogging, and reduce manual handling.

An immobilized endoglycosidase enables one-step Fc glycan conjugation for homogeneous ADC production with fewer enzyme impurities.

Controlled solvent evaporation drives nano-objects toward stiffer hydrogel zones, creating surface density gradients for chips, sensors, and diagnostics.

CRISPR-Cas9 capture complexes in mixed microfluidic channels isolate ctDNA from small plasma volumes without altering the DNA.

A polymer-immobilized NAD(P) enzyme cascade with transition metal mediators improves sensor stability, sensitivity, and rapid clinical analyte measurement.

A polymer-immobilized NAD(P)+ enzyme cascade uses a transition metal mediator to deliver stable, sensitive electrochemical analyte monitoring.

Candida antarctica lipase enables lower-temperature fatty amidoalkyldialkylamine synthesis with high yield, less excess amine, and fewer effluents.

A covalently linked block copolymer diffusion barrier avoids polymer-mixing issues while maintaining analyte permeability and sensor stability.

Synthetic random heteropolymers mimic enzyme active sites while resisting denaturation under harsh processing and high-temperature reaction conditions.

A silane-linked mediator in a sol-gel enzyme electrode limits mediator leakage while preserving mobility for faster electron transfer.

Ex vivo exposure of isolated immune cells to restrained tumor cells boosts tumor-specific responses while limiting systemic adverse effects.

Transition-metal redox mediators and polymer-immobilized NAD(P) enzymes improve sensor stability, sensitivity, and rapid analyte measurement.

A co-immobilized NAD(P) enzyme cascade with metal mediators improves sensor stability and measurement accuracy for glucose and related analytes.

Transition metal mediators and enzyme cascades enable stable, rapid, and clinically accurate electrochemical sensing of NAD(P)+ analytes.

A polymer-immobilized NAD(P) enzyme cascade uses a metal-complex mediator to improve stable, rapid electrochemical sensing of glucose, alcohol, and β-hydroxybutyrate.

Coupled dehydrogenase and oxidoreductase layers use transition metal mediators to improve stability and deliver accurate analyte readings fast.

Coupled dehydrogenase, oxidoreductase, and metal-complex mediator layers improve stable, sensitive analyte sensing in biological fluids.

Cell lysate enzymes immobilized in PAM hydrogel degrade extracellular antibiotic resistance genes while improving stability and reuse in water treatment.

Catechins are enriched on disposable macroporous resin, then oxidized by free PPO to raise theaflavin yield while cutting cost and waste.

A staged growth, fermentation, separation, and gel-mixing process protects microorganisms in biofertiliser during storage and adverse conditions.

Alkaline phosphatase staining makes hUC-MSC immune protein secretion visible by microscopy for simpler quality control.

Natural enzymes denature during high-temperature, solvent-based processing; random heteropolymers preserve catalytic activity and stabilize reaction intermediates.

A water-soluble polymer embeds functional proteins to trap VOCs, simplifying production and supporting immediate use and long-term storage.

A single-layer block copolymer combines hydrophilic and hydrophobic blocks to control analyte transfer without tedious multi-polymer barrier preparation.

Directed-evolved TPL enzymes maintain activity at high phenolic substrate concentrations, enabling up to 200 g/L L-tyrosine in 24 hours.

Tumor-antigen-loaded particles activate scarce, low-activity T cells before expansion and reinfusion to improve cancer-cell recognition.

Transpeptidation links peptides to encoding nucleic acids without puromycin linker preparation, preserving peptide structure for efficient screening.

Filtration, pH-controlled crystallization, and recyclable toluene extraction isolate amoxicillin while recovering phenylacetic acid.

See how one retroviral particle co-delivers Cas9 mRNA, guide RNA, and repair templates to address cargo limits in gene editing.