Development of a new phosphorescence sensor based on surface molecularly imprinted Mn-doped ZnS quantum dots for detection of melamine in milk products.

This paper presents a novel room temperature phosphorescence sensor (IMIPs-ZnS QDs RTP sensor) based on inorganic surface molecularly imprinted polymers and Mn-doped ZnS quantum dots (QDs) for the rapid detection of trace melamine (MEL) in commercial milk products. The surface of Mn-ZnS QDs was modified with 3-(mercaptopropyl) trimethoxy silane (MPTS). Then, MEL, 3-aminopropyltriethoxysilane (APTES) and tetraethoxysilane (TEOS) were used as a template/target molecule, functional monomer, and cross-linker, respectively.

Molecularly Imprinted Solid-Phase Extraction Sorbents for the Selective Extraction of Drugs from Human Urine.

Development of molecularly imprinted solid-phase extraction (MISPE) sorbents for the removal of drugs from human urine is described. MISPE sorbents are synthesized through free radical polymerization mechanism and non-covalent imprinting approach. After the completion of the polymerization, bulk polymer is ground using an analytical mill and then wet-sieved.

Spectrofluorimetric determination of atenolol from human urine using high-affinity molecularly imprinted solid-phase extraction sorbent.

This study presents a novel, sensitive and selective molecularly imprinted solid-phase extraction (MISPE)-spectrofluorimetric method for the removal and determination of atenolol from human urine. Molecularly imprinted and non-imprinted polymers were synthesized thermally using a radical chain polymerization technique and used as solid-phase extraction sorbents. Acrylic acid ethylene glycol dimethacrylate, dibenzoyl peroxide and dichloroethane were used as a functional monomer, cross-linker, initiator and porogen, respectively.

Preconcentration of indapamide from human urine using molecularly imprinted solid-phase extraction.

A simple, sensitive, and selective molecularly imprinted solid-phase extraction and spectrophotometric method has been developed for the clean-up and preconcentration of indapamide from human urine. Molecularly imprinted polymers were prepared by a non-covalent imprinting approach using indapamide as a template molecule, 2-(trifluoromethyl) acrylic acid as a functional monomer, ethylene glycol dimethacrylate as a crosslinker, N,N-azobisisobutyronitrile as a thermal initiator and acetonitrile as a porogenic solvent. A non-imprinted polymer was also prepared in the same way, but in the absence of template.

Development of a molecularly imprinted solid-phase extraction sorbent for the selective extraction of telmisartan from human urine.

A novel molecularly imprinted solid-phase extraction with spectrofluorimetry method has been developed for the selective extraction of telmisartan from human urine. Molecularly imprinted polymers were prepared by a noncovalent imprinting approach through UV-radical polymerization using telmisartan as a template molecule, 2-dimethylamino ethyl methacrylate as a functional monomer, ethylene glycol dimethacrylate as a cross-linker, N,N-azobisisobutyronitrile as an initiator, chloroform as a porogen. Molecularly imprinted polymers and nonimprinted control polymer sorbents were dry-packed into solid-phase extraction cartridges, and eluates from cartridges were analyzed using a spectrofluorimeter.

A novel solid-phase extraction-spectrofluorimetric method for the direct determination of atenolol in human urine.

A novel, simple, sensitive and selective solid-phase extraction (SPE)-spectrofluorimetric method has been developed for the determination of atenolol (ATE) in human urine. Because an extraction procedure is required to isolate ATE or eliminate the interfering molecules present in complex human urine for the direct spectrofluorimetric determination, a pH-sensitive poly(acrylic acid-ethylene glycol dimethacrylate) [poly(AA-EGDMA)] hydrogel was developed and used as a SPE adsorbent. Some factors affecting the ATE extraction efficiency, such as washing solvent type and volume, and the volume of elution solvent were optimized.

A novel spectrofluorimetric method for the determination of calcitonin in ampules through derivatization with fluorescamine.

In this study, a simple, sensitive and selective spectroflourimetric method has been developed for the determination of salmon calcitonin (sCT) in ampules. The method is based on the reaction between sCT and fluorescamine at pH 8.5 in borate buffer, resulting in a highly fluorescent derivative.

Release characteristics of salmon calcitonin from dextran hydrogels for colon-specific delivery.

Biodegradable dextran hydrogels were synthesized by crosslinking dextran (T-70) with epichlorohydrin (ECH) for the in vitro colon-specific delivery of salmon calcitonin (sCT). Crosslinking reaction was performed in 2.8 M NaOH solution both in the presence and absence of ethanol at 10 and 23 degrees C.

Quantitative determination of ketoprofen in gels and ampules by using flow-injection UV spectrophotometry and HPLC.

A flow-injection UV spectrophotometric method for the determination of ketoprofen in gels and ampules was developed. Quantitative determination of ketoprofen was realized by using distilled water as a carrier for gels and citrate buffer, pH 6.5, for ampules at 261 nm.

Quantitative determination of ambroxol in tablets by derivative UV spectrophotometric method and HPLC.

A derivative UV spectrophotometric method for the determination of ambroxol in tablets was developed. Determination of ambroxol in tablets was conducted by using first-order derivative UV spectrophotometric method at 255 nm (n = 5). Standards for the calibration graph ranging from 5.

Diclofenac sodium releasing pH-sensitive monolithic devices.

A non-steroidal anti-inflammatory agent, diclofenac sodium (DFNa), was incorporated into the pH-sensitive monolithic systems prepared by crosslinking/copolymerization of 2-hydroxyethyl methacrylate (HEMA) with acrylate-based acidic and basic comonomers, i.e. acrylic acid (AA) and dimethylaminoethyl methacrylate (DMAEMA).