Biocide TRIZ Cases

A polymer blend membrane controls pheromone release rates without increasing membrane thickness.

Developing crystalline form I of Febuxostat resolves the contradiction between limited solubility and formulation stability found in prior art.

A composition of citrus flavonoids and cationic surfactants infiltrates lice tracheae to block oxygen uptake.

Pyrimidine sulfonamide compounds modulate chemokine receptor activity to treat inflammatory diseases.

A topical preparation combining linalool, tea tree oil, and Tris-EDTA delivers rapid bactericidal activity against ocular pathogens.

A biodegradable polymer mixture reduces urea granulate compressibility, caking, and re-crystallization while avoiding toxicity and pH changes.

A Cannabaceae seed flour mixture kills Tenebrionidae insects through natural toxicity.

Benzothiophene hydroxamic acid derivatives resolve potency and bioavailability limitations by selectively inducing apoptosis in neoplastic cells.

Compositions combining 1-hexanol and decanal activate human-sensitive glomeruli, sustaining attractant effects where conventional agents fail rapidly.

Chlorite reduces activated macrophages to stabilize disease progression in ALS, MS, and Alzheimer's patients.

A food-grade coating combines liquid smoke with xanthan gum to protect dry-cured hams from mite infestations.

Using E,E-8,10-dodecadienyl acetate for mating disruption reduces release positions while maintaining control effectiveness.

Optimized pH and ion fractions stabilize high-concentration aqueous biocides against solid separation at low temperatures while eliminating VOC solvents.

Oxime-containing acyl guanidine derivatives inhibit beta-secretase activity, reducing beta-amyloid peptide accumulation in the brain.

Disrupting the fbp gene in Bacillus reduces fructose bisphosphatase activity, redirecting metabolic flux to boost purine nucleoside fermentation yields.

Specific particle sizing reduces pesticide application rates while maintaining broad-spectrum control against cryptic soil-dwelling pests and diseases.

Novel cyclic derivatives modulate chemokine receptor activity to resolve contradictions between ion channel selectivity, safety, and oral bioavailability.

Controlling stabilizer levels in ivermectin feed premixes adjusts the pH to prevent acid and base catalyzed decomposition of active ingredients.

Silver ion-exchanged glass beads resolve microbial contamination in metallic coatings while maintaining luster.

Formula One compounds overcome pest resistance to protect crop yields through novel molecular structures.

Substituted beta-lactam compounds resolve glaucoma treatment limitations by acting as prostaglandin EP2 receptor agonists to reduce intraocular pressure.

Inhibiting saccharopine dehydrogenase via RNA interference disrupts lysine biosynthesis in fungi and oomycetes.

Combines pyridazine and pyrrolidinone derivatives for synergistic weed control.

HDAC inhibitors increase histone acetylation to restore long-term memory access despite irreversible neuronal loss.

Novel protein kinase inhibitors designed for oral bioavailability targeting MAPK and CK pathways.

Optimized oxygenated monoterpenoid ratios achieve therapeutic antibacterial potency at low concentrations, avoiding toxicity and resistance issues.

Microcapsules coated with nonionic polysaccharide polymer adhere to biofilms for targeted delivery of functional materials.

Composite walls prevent leakage and degradation of encapsulated oils in high ethanol and surfactant environments.

Pyrimidinium compounds manage pest resistance through synergistic mixtures that maintain efficacy while reducing environmental impact.

Segmenting alpha2 receptor subtypes enables selective binding that reduces sedation and hypotension while maintaining pain relief.

Colloidal silica adjusts viscosity in peroxidised lipids, enabling spray application that lines buccal tissues and alleviates dry mouth symptoms.

A ready-to-use liquid larvicide composition combines Bacillus thuringiensis fermentate with propionic acid and water.

Heterocyclic compounds reduce nematode populations without destroying plants, preserving crop yield.

Amino-heteroaryl prokineticin 1 receptor antagonists block specific signaling pathways to modulate gastrointestinal function.

Single picolinamide active ingredient replaces multiple specialized fungicides, reducing application complexity and cost while maintaining effective coverage.

Halogen substitution at the 2-position of benzoxazinones boosts herbicidal activity at low application rates while preserving crop plant compatibility.

Combining propyl propane thiosulfinate with propyl propane thiosulfonate lowers treatment costs while maintaining regulatory compliance for parasite control.

Merging distinct modes of action reduces resistance development while lowering required application dosages.

Ionizable salt stabilizes amphiphilic block copolymer micelles, preventing rapid drug release and maintaining stability for extended periods.

Novel quinoxaline derivatives inhibit phosphodiesterase type 9 to stabilize intracellular cyclic guanosine monophosphate levels.

White chromium composite plating layer with nano-needle structure eliminates hexavalent chromium toxicity while providing durable antibacterial protection.

Integrates chromenone derivatives with retinoids to enhance wrinkle reduction while minimizing skin irritation through synergistic cellular modulation.

Bacillus subtilis strain DSM 32685 inhibits pathogenic bacteria growth and degrades non-starch polysaccharides in animal feed.

A concentrated antimicrobial solution and cream using Muscodor crispans volatile compounds to treat ringworm on skin and surfaces.

Serum-free culture medium expands endothelial progenitor cells using specific growth factors for therapeutic applications.

Optimizing iron concentration and carbon-to-nitrogen ratios in the growth medium reduces preparation time while increasing fungal resistance to abiotic stress.

Gαs-coupled dopamine receptor D1 agonists inhibit YAP/TAZ function in mesenchymal cells.

A sublingual coated tablet design uses a drug-free compressed core to isolate the active substance in the coating layer.

Merging distinct fungicidal compounds into synergistic mixtures reduces dosage rates while maintaining broad-spectrum activity against phytopathogenic fungi.