Potassium Iodate Research Articles

Synthesis of polyfluoroiodoarenes from polyfluoroarenethiols and KIO<sub>3</sub>

By heating polyfluoroarenethiols with potassium iodate at 150–235°C in ampoules, a number of iodopolyfluoroarenes were obtained as the main products along with dipolyfluoroarylsulfanes.

Iodine-Enriched Urea Reduces Volatilization and Improves Nitrogen Uptake in Maize Plants

Urea is the primary source of nitrogen (N) used in agriculture. However, it has a high N loss potential through volatilization. Various mechanisms can be employed to reduce N volatilization losses by inhibiting urease. When added to urea, iodine (I) has high potential for this purpose. Thus, this study aimed to determine whether adding I to urea reduces volatilization losses and increases N uptake in maize plants. Maize plants were cultivated in greenhouse conditions for 36 days. Urea treatments were applied at 15 days of testing, including iodine-enriched urea, conventional urea, and no urea application. Additionally, a study concerning N volatilization from urea was conducted using the same treatments under the same environmental conditions. Iodine was incorporated and adhered to urea, at an I concentration of 0.2%, using potassium iodate (KIO3). Under controlled conditions and over a short period of time, it was observed that the application of iodine-enriched urea increased the chlorophyll b content, root N accumulation, and total N accumulation in maize plants compared with conventional urea. Moreover, iodine-enriched urea reduced N losses from volatilization by 11% compared with conventional urea. The reduction in N volatilization correlated positively with the increased chlorophyll b, total chlorophyll, root N accumulation, and total N accumulation favored by the iodine-enriched urea treatment. Our findings demonstrated that adding I to urea is an efficient and promising strategy to reduce N losses and increase N uptake in plants.

Superior Electrochemical Sensor Application of Co3O4/C Heterostructure in Rapid Analysis of Anticancer Drug Palbociclib in Pharmaceutical Formulations and Biological Fluids.

In this work, we report a study examining how different salt concentrations affect the structure and electrochemical performance of two Co3O4/C materials designed for the fabrication of an easy, cheap, fast, safe, and useful electrochemical sensor for the detection of Palbociclib (PLB). Co3O4 nanoparticles were successfully created by encapsulating them in N-doped amorphous carbon matrices by using the molten salt-assisted approach. In this process, different amounts of potassium iodate and zeolitic imidazolate framework-12 (ZIF-12) were used, followed by pyrolysis at 800 °C. Optimum Co3O4 embedded porous carbon structures were obtained, and the composite with the highest electrochemical properties was modified to a glassy carbon electrode (GCE) surface for PLB detection. The linear response spanned from 1.0 to 5.0 μM, featuring a limit of detection (LOD) of 0.122 μM and a limit of quantification (LOQ) of 0.408 μM; the correlation coefficient was calculated as 0.995. The high sensitivity of the method in detecting PLB in pharmaceutical samples and human urine demonstrated its feasibility, with recovery percentages ranging from 99.3% to 101.3% and relative standard deviation (RSD) values of <3%. Therefore, this technique will make a significant contribution to monitoring and improving existing cancer treatment options.

Spectrophotometric Assessment of Pyrocatechol Drug Employing Oxidative Coupling Reaction with 4-amino antipyrine as a Model of Pharmaceutical Compounds .

A rapid, simple, sensitive, and higher stability spectrophotometric method was developed the determine that it is stable Pyrocatechol drug in pure and pharmaceutical preparations. The method is based on an oxidative coupling reaction among Pyrocatechol drug and 4-amino antipyrine (4AAP) in the presence of potassium iodate (KIO3) in an acid medium to form a color complex that stable violet dye and a maximum absorption at 505 nm. The best optimum conditions and other analytical factors have been evaluated. A calibration curve of absorbance of several concentrations that obey the law of Beer-Lambert over the range concentration of pyrocatechol drug 10 to 100 mg/L, with (LoD =1.2*10-4 mg/L), (LoQ=3.4*10-4 mg/L), The relative standard deviations RSD% of the proposed methods were less than 0.68%). In contrast, recovery average and determination parameters are 99.9%. The method was used successfully for the determination of drugs in a pharmaceutical preparation with the best accuracy and precision. At range about 99.1 to 100.2% with RSD less than 0.3%. The analytical result for the estimation of the pure drug is presented together with the use of the proposed process for the analysis of some commercial pharmaceuticals. The data compare favorably with those of official and reported ways.

Efficient Synthesis and Iodine-Functionalization of Pyrazoles via KIO3/PhSeSePh System under Acidic Conditions.

This manuscript reports a novel method for the direct iodination of the C-4 pyrazole ring generated in situ by the reaction of 1,1,3,3-tetramethoxypropane and various hydrazines. In this approach, potassium iodate (KIO3) is used as the iodinating agent and (PhSe)2 is used as catalysts under acidic conditions. This protocol provides a convenient method for the efficient synthesis of 4-iodo-1-aryl-1H-pyrazoles, valuable intermediates for several different coupling reactions.

The Role of Potassium Iodate in Mitigating the Damages of Water Deficit in Coffee Plants

The Role of Potassium Iodate in Mitigating the Damages of Water Deficit in Coffee Plants

Application of Monoclonal Antibodies against Naturally Occurring Bioactive Ingredients.

Monoclonal antibodies (Mabs) are widely used in a variety of fields, including protein identification, life sciences, medicine, and natural product chemistry. This review focuses on Mabs against naturally occurring active compounds. The preparation of Mabs against various active compounds began in the 1980s, and now there are fewer than 50 types. Eastern blotting, which was developed as an antibody staining method for low-molecular-weight compounds, is useful for its ability to visually represent specific components. In this method, a mixture of lower-molecular-weight compounds, particularly glycosides, are separated by thin-layer chromatography (TLC). The compounds are then transferred to a membrane by heating, followed by treatment with potassium periodate (KIO4) to open the sugar moiety of the glycoside on the membrane to form an aldehyde group. Proteins are then added to form Schiff base bonds to enable adsorption on the membrane. A Mab is bound to the glycoside moiety on the membrane and reacts with a secondary antibody to produce color. Double Eastern blotting, which enables the simultaneous coloration of two glycosides, can be used to evaluate quality and estimate pharmacological effects. An example of staining by Eastern blotting and a component search based on the results will also be presented. A Mab-associated affinity column is a method for isolating antigen molecules in a single step. However, the usefulness of the wash fractions that are not bound to the affinity column is unknown. Therefore, we designated the wash fraction the "knockout extract". Comparing the nitric oxide (NO) production of a glycyrrhizin (GL)-knockout extract of licorice with a licorice extract revealed that the licorice extract is stronger. Therefore, the addition of GL to the GL-knockout extract of licorice increased NO production. This indicates that GL has synergic activity with the knockout extract. The GL-knockout extract of licorice inhibited high-glucose-induced epithelial-mesenchymal transition in NRK-52E cells, primarily by suppressing the Notch2 pathway. The real active constituent in licorice may be constituents other than GL, which is the causative agent of pseudohyperaldosteronism. This suggests that a GL-knockout extract of licorice may be useful for the treatment of diabetic nephritis.

Enhanced antimicrobial activity of photocatalytic titanium oxide upon formation of composites with polyaniline via an eco-friendly and facile microwave synthesis approach

This study proposes inexpensive antimicrobial polyaniline-titanium oxide (PANI-TiO2) samples prepared through eco-friendly enhanced microwave (MW) synthesis with 93 W applied over 10 min in aqueous 1.25 M hydrochloric acid media (HCl) using potassium iodate (KIO3) as oxidising agent, an approach suitable for industrial scale up production of PANI polymers at room temperature. The PANI-TiO2 samples are produced in the presence of 5–20 wt% of TiO2 in the initial reaction mixture along with aniline monomer by both the enhanced MW method and a classical chemical synthesis (CS) method at room temperature. The nanocomposites showed lower conductivity than pure PANI, slightly higher conductivity was observed in the MW prepared PANI-TiO2 in comparison to CS prepared PANI-TiO2. This result can be correlated with the observation that the optical absorbance of MW PANI-TiO2 samples were notable higher than for CS PANI-TiO2, which may be due to the presence of a greater amount of polarons present in the samples prepared by the enhanced MW method. MW PANI-TiO2 samples were equally active against both Gram-negative E. coli and Gram-positive S. aureus bacteria, in contrast to the CS PANI-TiO2 samples, which could be due to presence of short-chain fragments in the CS samples as confirmed by Fourier-transform infrared (FTIR) spectroscopy. The incorporation of PANI particles in TiO2 showed enhanced antimicrobial activity compared to pure TiO2, with greater antifungal activity. Our study indicates that a facile, low-cost, and green enhanced MW method can be used for preparation of the advanced antimicrobial PANI-TiO2 nanocomposites for biomedical applications.

Effect of iodine species on biofortification of iodine in cabbage plants cultivated in hydroponic cultures

Iodine is an essential trace element in the human diet because it is involved in the synthesis of thyroid hormones. Iodine deficiency affects over 2.2 billion people worldwide, making it a significant challenge to find plant-based sources of iodine that meet the recommended daily intake of this trace element. In this study, cabbage plants were cultivated in a hydroponic system containing iodine at concentrations ranging from 0.01 to 1.0 mg/L in the form of potassium iodide or potassium iodate. During the experiments, plant physiological parameters, biomass production, and concentration changes of iodine and selected microelements in different plant parts were investigated. In addition, the oxidation state of the accumulated iodine in root samples was determined. Results showed that iodine addition had no effect on photosynthetic efficiency and chlorophyll content. Iodide treatment did not considerably stimulate biomass production but iodate treatment increased it at concentrations less than 0.5 mg/L. Increasing iodine concentrations in the nutrient solutions increased iodine content in all plant parts; however, the iodide treatment was 2–7 times more efficient than the iodate treatment. It was concluded, that iodide addition was more favourable on the target element accumulation, however, it should be highlighted that application of this chemical form in nutrient solution decreased the concetrations of selected micoelement concentration comparing with the control plants. It was established that iodate was reduced to iodide during its uptake in cabbage roots, which means that independently from the oxidation number of iodine (+ 5, − 1) applied in the nutrient solutions, the reduced form of target element was transported to the aerial and edible tissues.

A quantitative analysis of vitamin C in fruits, khat (Catha edulis), and pharmaceutical tablets using potassium iodate titration

Vitamin C, or ascorbic acid, is an essential antioxidant in various resources, such as pharmaceutical tablets, fruits, and vegetables. The human body cannot synthesize it by itself. This research aims to measure the vitamin C content in 29 commonly assessable compressed tablets, effervescent tablets, fruits, and khat (Catha edulis) leaves that are found in the Yemeni local markets. This study used a redox titration method with potassium iodate. These results reveal confirmed European and American standards and no significant difference between the measured vitamin C content in the commercial tablet (p &lt;0.05) and the amount stated on the product label, as well as the highest amount of vitamin C content in fruits in guava (111.21 mg/100 g), while the lowest amount of vitamin C is in apple (8.72 mg/100 g).

Assessment of sorbitol clearance in induced acute liver failure

The study of substance clearance plays an important role in the diagnosis of liver pathologies. Increased or decreased clearance of certain substances may indicate hepatobiliary disorders, including at the initial stages of the development of such pathologies, which allows us to evaluate the predictive potential of these assessment methods as high. The scientific literature provides detailed and statistically proven data on the use of substances such as galactose, amidopyrine, sorbitol and others in diagnostic protocols. Each substance is characterized by its own level of clearance, which allows one to obtain a comprehensive picture of the functioning of the hepatobiliary system. However, for most of the above exogenous substances, information in the scientific literature is either indicated in relation to humane medicine, or consists of pilot studies on a small number of animals, which requires additional testing of this kind to develop a statistically reliable array of data obtained. The purpose of this study is to conduct an experimental study aimed at studying changes in the pharmacokinetics of exogenous sorbitol in the blood plasma of laboratory animals with acute liver failure. The level of sorbitol was determined by the colorimetric Corcoran and Page method with modification (using potassium periodate and chromotropic acid, the method takes into account the calculated sorbitol indicator from the sum of polyols) using a UV-100 spectrophotometer (manufacturer – Shanghai Mapada Instruments Co., Ltd., China) for 12 hours (step – 2 hours) in blood plasma deproteinized using 0.4 M lithium perchlorate, obtained by venipuncture of the tail vein. Comparing pharmacokinetic curves with each other, it should be noted that in animals with acute liver failure, the graphical representation of sorbitol levels is similar to the inverse exponential, characterized by a sharp systematic decrease, while in clinically healthy animals the graphical representation of sorbitol levels is similar to the branch of a parabola, characterized by “smoothness” » reduction. The pharmacokinetic curves obtained in this study, which describe the levels of exogenous sorbitol in the blood plasma, can be used in the future as one of the methods for the early diagnosis of such pathologies.

Green and Versatile High-Throughput Microwell Oxidation-Based Spectrophotometric Methods for Determination of Galidesivir in Capsules.

Galidesivir (GDV) is a promising new antiviral drug for the potent and safe treatment of a broad spectrum of viral diseases, including COVID-19. In the literature, no analytical method exists for the determination of GDV in bulk and dosage form. The aim of this study was the development of versatile green and simple microwell spectrophotometric methods (MW-SPMs) for the determination of GDV in its bulk form and capsules. Three MW-SPMs were developed involving the oxidation of GDV by ammonium metavanadate (AMV), chromium trioxide (CTO), and potassium iodate (PIO) in an acid medium. The reactions were carried out in 96-well plates at room temperature and the absorbances of chromogenic reaction products were measured by an absorbance microplate reader at 780, 595, and 475 nm for AMV, CTO, and PIO, respectively. Variables influencing the reactions were carefully investigated and optimized. Linear relations with excellent correlation coefficients (0.9991-0.9997) were found between the absorbances and GDV concentrations in the range of 25-500 µg/mL. The LODs were ≥8.3 µg/mL. The accuracy and precision of the three MW-SPMs were confirmed by recovery and replicate analysis, respectively. The recovery values were 98.6-101.2% and the RSDs were ≤1.02%. The proposed MW-SPMs were successfully applied to the analysis of GDV in bulk drug and capsules with high accuracy and precision. The greenness of the MW-SPMs was confirmed by three comprehensive metric tools. The proposed MW-SPMs combined the inherent advantages of microwell-based analysis and the use of common laboratory reagents for the reactions involved. These advantages include high-throughput, ready automation, reduced sample/reagent volume, precise measurements, and versatility. The advantages of the use of common laboratory reagents include availability, consistency, compatibility, safety, and cost-effectiveness. Overall, the proposed MW-SPMs are versatile valuable tools for the quantitation of GDV during its pharmaceutical manufacturing.

Fabrication of molybdenum disulphide / carbon paste (MoS2/CP) nanocomposite as a modified platinum electrode for electrocatalytic oxidation of benzyl alcohol in biphasic electrolysis

Alcohol to aldehyde conversion is a significant industrial process. Herein, we developed the biphasic method for converting the alcohols to aldehydes and ketones in the presence of potassium iodate as an electrocatalytic mediator. This transformation is obtained after 3.5 h at room temperature using the Platinum (Pt) metal electrodes decorated with molybdenum disulphide (MoS2) and Carbon Paste (CP). A thin layer of MoS2 and CP helps to evenly deposit the Pt metal onto the surface, resulting in a significant surface improvement. The electrochemical properties of the modified platinum electrodes were analyzed by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The physicochemical properties of the modified electrodes were studied by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. This method has been applied to the electrochemical oxidation of benzyl alcohol via interphasic in iodate free radicals. The cyclic potentiometric studies showed the electrocatalytic activity of the Pt-MoS2-CP electrode was higher than the Pt–MoS2 electrode in terms of the ability to convert benzyl alcohol to benzaldehyde. High electrocatalytic activity, rapid current response, and stable catalytic activity were all characteristics of the chemically modified electrode.

Dual single atomic Fe-Ni sites in N‑doped nanoporous carbon for high-efficiency potassium periodate activation toward pollutant abatement

Diatomic catalysts (DACs) with atomically isolated metal pairs hold the potential for activating potassium periodate (PI) in sustainable pollution control, yet their synthesis poses a significant challenge. In this study, Fe/Ni species anchored to a nitrogen-doped carbon as diatomic catalysts (FeNi-NC DACs) were precisely synthesized by direct carbonization of metal–organic frameworks (MOFs) assembled by Fe/Ni-doped ZnO nanoparticles and used for the effective decomposition of organic pollutants through PI activation. As anticipated, FeNi-NC exhibited superior catalytic properties due to the abundance of adjacent bimetallic active sites (Fe/Ni-Nx), rich doped nitrogen, high specific surface area, and electron transport conductivity, surpassing single-atom Fe-NC and Ni-NC, as well as nonmetallic NC catalysts. Free radical quenching, electron paramagnetic resonance, and electrochemical experiments have shown that the FeNi-NC/PI system can oxidize organic compounds through non-free radical oxidation pathways, including singlet oxygen (1O2) oxidation and mediated electron transfer processes. Electron transfer mediated by FeNi-NC/PI* complexes is the primary mechanism for organic oxidation. Additionally, the FeNi-NC catalyst demonstrated remarkable stability in both inorganic-containing and real water samples, as well as in continuous-flow microreactors. This study introduces a novel approach for designing highly efficient DACs and offers fundamental insights into the mechanism of PI-activated oxidation of organic pollutants.

Synergistic Antifungal Activity of Dialdehyde Chitosan Loaded with Copper Metal‐Organic Framework (Cu‐MOF)

AbstractFungal resistance and the environmental degradation posed by conventional fungicides necessitate the need to develop new antifungal agents that can inhibit fungal growth. This study sought to prepare biofungicides by leveraging on the antifungal activity of copper‐metal organic framework (Cu‐MOF) and dialdehyde chitosan (Cs) isolated from black soldier flies (BSF). Cs were oxidized using potassium periodate to obtain dialdehyde Cs (OCs) and thereafter, Cu‐MOF was loaded resulting in Cu‐MOF‐OCs. Fourier Transform Infrared spectrophotometer (FT‐IR) and powder X‐ray diffraction (XRD) confirmed the presence of carbonyl functional groups in OCs and sharp intense peaks associated with Cu that interacted. The changes in surface morphology and the presence of Cu in the MOFs as obtained with Scanning Electron Microscope‐ Energy Dispersive X‐ray (SEM‐EDX), indicated the successful loading of Cu‐MOF on the oxidized Cs. Thermogravimetric analysis (TGA) showed a loss of approximately 31.51 % of the loaded OCs and 40.72 % framework around ∼200 to ∼300 °C and ∼410 to ∼475 °C respectively. The antifungal activity of OCs, Cu‐MOF, and Cu‐MOF‐OCs against Aspergillus brasiliensis and Candida albicans was performed using the plate count method and the results suggested that MOF modulated the antifungal activity exerted by the OCs.

Finely-Tuning Chemiluminescent Color of CdTe Nanocrystals and Its Application for Near-Infrared Semi-Automatic Immunoassay.

Chemiluminescence (CL), especially commercialized CL immunoassay (CLIA), is normally performed within the eye-visible region of the spectrum by exploiting the electronic-transition-related emission of the molecule luminophore. Herein, dual-stabilizers-capped CdTe nanocrystals (NCs) is employed as a model of nanoparticulated luminophore to finely tune the CL color with superior color purity. Initialized by oxidizing the CdTe NCs with potassium periodate (KIO4), intermediates of the reactive oxygen species (ROS) tend to charge CdTe NCs in both series-connection and parallel-connection routes and dominate the charge-transfer CL of CdTe NCs. The CdTe NCs/KIO4 system can exhibit color-tunable CL with the maximum emission wavelength shifted from 694 nm to 801 nm, and the red-shift span is over 100 nm. Both PL and CL of each of the CdTe NCs are bandgap-engineered; the change in the NCs surface state via CL reaction enables CL of each of the CdTe NCs to be red-shifted for ∼20 nm to PL, while the change in the NCs surface state via labeling CdTe NCs to secondary-antibody (Ab2) enables CL of the CdTe NCs-Ab2 conjugates to be red-shifted for another ∼20 nm to bare CdTe NCs. The CL of CdTe753-Ab2/KIO4 is ∼791 nm, which can perform near-infrared CL immunoassay and semi-automatically determined procalcitonin (PCT) on commercialized in vitro diagnosis (IVD) instruments.

Salt production and iodization practices among artisanal salt producers in selected districts within the Greater Accra and Central Regions of Ghana

BackgroundThis study was conducted to assess salt production and iodization practices by artisanal salt producers located at six districts across Greater Accra and Central regions. MethodsOne Hundred and Sixty-Six (166) salt miners in Greater Accra and Central Regions were interviewed using a structured questionnaire and their production sites inspected for salt iodization practices. ResultsThe study revealed that salt iodization is not practiced among majority (69.28 %) of artisanal salt producers. They were conversant with salt iodization (93.98 %) and had fair knowledge on the health effects on consumers when iodine is absent in salt. Some of the producers attributed the nonadherence to the mandatory salt iodization to the unavailability of potassium iodate/iodide on the market. All artisanal salt producers interviewed utilise the solar evaporation method for salt production. The evaporation is done on tarpaulin/polyethylene lined pans and concrete pans. The tarpaulin/polyethylene lined pans were predominantly used in Greater Accra, and concrete pans in Central region. ConclusionFor Ghana to increase availability of iodized salt on the market and improve household consumption of iodized salt, regulatory authorities need to enforce the laws and regulations on salt iodization and also create the enabling environment for artisanal salt producer to have access to potassium iodate for production.

Kinetic perspectives for the degradation of oxacillin: A penicillanic acid derivative

Oxidation of oxacillin, a penicillanic acid derivative, has been predicted by monoperiodatocuprate [MPC (III)] at 25°C with 0.10 mol dm-3 ionic strength, in an aqueous alkaline medium by UV/Visible spectrophotometric analysis, for which 1:4 stoichiometry of oxacillin: MPC (III) is visible. The appearance of a sharp peak by the spectrophotometer confirmed the formation of the complex. The reaction products have been recognized using spectral reports from the FT-IR, LC-MS, melting point, and other spot tests. A pseudo-first-order reaction has been confirmed for the oxidant, fractional order for the substrate, and alkali, even though periodate claimed a delaying effect due to the accumulation of periodate ions from both potassium periodate and monoperiodatocuprate as a common ion effect. The primary active species in the alkaline medium [Cu(H2IO6)(H2O)2] was discovered to be monoperiodatocuprate [MPC (III)]. To figure out the activation and thermodynamic parameters, it is helpful to know the uncatalyzed rate constants, the slow step rate constants, and the equilibrium constants. We have evaluated the dependence of reaction rates on different temperatures. We have calculated rate constants using absorbance data collected from the UV/visible spectrophotometer. We have thoroughly examined the potential rate constant derivation and a plausible mechanism that could explain the experimental findings.

Development of a Spectrophotometric Technique for The Estimation of Sulfamethoxazole (SMX) in its Pure also in Pharmaceutical Formulatio, using organic reagent (A1)

A sensitive, simple, as well as accurate spectrophotometric technique to the estimation of Sulfamethoxazole (SMX) drug in pure also pharmaceutical formulations was developed. It was created by the reaction of (SMX) and organic reagent (A1) after oxidation by iron chloride and potassium periodate in acidic medium. The absorption of the product of SMX and A1 was measured at 423 nm. Linearity ranged between (0.5-22.5 μg. mL-1), molar absorptivity was (6.839 *10+3L / mol.cm), limits of detection and quantification were (0.204, 0.612 μg/ml ), respectively, the method was applied successfully to the estimation of SMX in pure and pharmaceutical formulations.

Development of 3D Printed Biodegradable, Entirely X-ray Visible Stents for Rabbit Carotid Artery Implantation.

Biodegradable stents are considered a promising strategy for the endovascular treatment of cerebrovascular diseases. The visualization of biodegradable stents is of significance during the implantation and long-term follow-up. Endowing biodegradable stents with X-ray radiopacity can overcome the weakness of intrinsic radioparency of polymers. Hence, this work focuses on the development of an entirely X-ray visible biodegradable stent (PCL-KIO3) composed of polycaprolactone (PCL) and potassium iodate via physical blending and 3D printing. The in vitro results show that the introduction of potassium iodate makes the 3D-printed PCL stents visualizable under X-ray. So far, there is inadequate study about polymeric stent visualization in vivo. Therefore, PCL-KIO3 stents are implanted into the rabbit carotid artery to evaluate the biosafety and visibility performance. During stent deployment, the visualization of the PCL-KIO3 stent effectively helps to understand the position and dilation status of stents. At 6-month follow-up, the PCL-KIO3 stent could still be observed under X-ray and maintains excellent vessel patency. To sum up, this study demonstrates that PCL-KIO3 stent may provide a robust strategy for biodegradable stent visualization.