Radioactive iodine in the management of medullary carcinoma of the thyroid.

Objectives: Although it is generally accepted that medullary thyroid cancer (MTC) cells do not take up iodine, there are reports indicating that this can occur. Additionally, the potential for radioactive iodine (RAI) to reduce the risk of recurrence within the thyroid bed following thyroid remnant ablation in MTC is uncertain. A systematic review was therefore undertaken.

Direct and Indirect Pathways of CdTeSe Magic-Size Cluster Isomerization Induced by Surface Ligands at Room Temperature.

The field of isomerization reactions for colloidal semiconductor magic-size clusters (MSCs) remains largely unexplored. Here, we show that MSCs isomerize via two fundamental pathways that are regulated by the acidity and amount of an incoming ligand, with CdTeSe as the model system. When MSC-399 isomerizes to MSC-422 at room temperature, the peak red-shift from 399 to 422 nm is continuous (pathway 1) and/or stepwise (pathway 2) as monitored in situ and in real time by optical absorption spectroscopy.

Transformations of Magic-Size Clusters via Precursor Compound Cation Exchange at Room Temperature.

The transformation of colloidal semiconductor magic-size clusters (MSCs) from zinc to cadmium chalcogenide (ZnE to CdE) at low temperatures has received scant attention. Here, we report the first room-temperature evolution of CdE MSCs from ZnE samples and our interpretation of the transformation pathway. We show that when prenucleation stage samples of ZnE are mixed with cadmium oleate (Cd(OA)), CdE MSCs evolve; without this mixing, ZnE MSCs develop.

Manipulating Reaction Intermediates to Aqueous-Phase ZnSe Magic-Size Clusters and Quantum Dots at Room Temperature.

It is not resolved which model describes better the aqueous-phase nucleation and growth of semiconductor quantum dots (QDs), the classical one-step one or the nonclassical multi-step one. Here, we design a room-temperature reaction to trap reaction intermediates in the prenucleation stage of ZnSe QDs (as a model system). We show that the trapped intermediate can transform to magic-size clusters (MSCs) via intra-molecular reorganization and can fragment to enable the growth of QDs.

A Real-Time In Situ Demonstration of Direct and Indirect Transformation Pathways in CdTe Magic-Size Clusters at Room Temperature.

The transformations of colloidal semiconductor magic-size clusters (MSCs) are expected to occur with only discrete, step-wise redshifts in optical absorption. Here, we challenge this assumption presenting a novel, conceptually different transformation, for which the redshift is continuous. In the room-temperature transformation from CdTe MSC-448 to MSC-488 (designated by the peak wavelengths in nanometer), the redshift of absorption monitored in situ displays distinctly continuous and/or step-wise behavior.

Size matters: Steric hindrance of precursor molecules controlling the evolution of CdSe magic-size clusters and quantum dots.

Unlabelled: Little is known about how to precisely promote the selective production of either colloidal semiconductor metal chalcogenide (ME), magic-size clusters (MSCs), or quantum dots (QDs). Recently, a two-pathway model has been proposed to comprehend their evolution; here, we reveal for the first time that the size of precursors plays a decisive role in the selected evolution pathway of MSCs and QDs. With the reaction of cadmium myristate (Cd(MA)) and tri-n-octylphosphine selenide (SeTOP) in 1-octadecene (ODE) as a model system, the size of Cd precursors was manipulated by the steric hindrance of carboxylic acid (RCOOH) additive.

A Two-Pathway Model for the Evolution of Colloidal Compound Semiconductor Quantum Dots and Magic-Size Clusters.

A fundamental understanding of formation pathways is critical to the controlled synthesis of colloidal semiconductor nanocrystals. As ultrasmall-size quantum dots (QDs) sometimes emerge in reactions along with magic-size clusters (MSCs), distinguishing their individual pathway of evolution is important, but has proven difficult. To decouple the evolution of QDs and MSCs, an unconventional, selective approach has been developed, along with a two-pathway model that provides a fundamental understanding of production selectivity.

Transformation Pathways in Colloidal CdTeSe Magic-Size Clusters.

A rarely studied transformation in colloidal ternary magic-size clusters (MSCs) is addressed. We report the first observation of the transformation from ternary CdTeSe MSC-399 to MSC-422, which occurs at room temperature. These two MSC types display sharp optical absorption resonances at 399 and 422 nm, respectively, and are related in that they are quasi isomers, together with their counterpart precursor compounds (PCs).

Transformation Pathway from CdSe Magic-Size Clusters with Absorption Doublets at 373/393 nm to Clusters at 434/460 nm.

Divergent interpretations have appeared in the literature regarding the structural nature and evolutionary behavior for photoluminescent CdSe nanospecies with sharp doublets in optical absorption. We report a comprehensive description of the transformation pathway from one CdSe nanospecies displaying an absorption doublet at 373/393 nm to another species with a doublet at 433/460 nm. These two nanospecies are zero-dimensional (0D) magic-size clusters (MSCs) with 3D quantum confinement, and are labeled dMSC-393 and dMSC-460, respectively.

Reversible Transformations at Room Temperature among Three Types of CdTe Magic-Size Clusters.

We report the first observation of the reversible transformations that occur among three types of CdTe magic-size clusters (MSCs) in dispersion at room temperature and discuss our understanding of the transformation pathway. The reversible transformations were achieved with CdTe prenucleation stage samples, which were prepared with reactions of cadmium oleate [Cd(OA)] and tri--octylphosphine telluride in 1-octadecene and were then dispersed in mixtures of toluene and a primary amine at room temperature. Three types of OA-passivated CdTe MSCs evolved, exhibiting sharp optical absorption singlets peaking at 371, 417, and 448 nm.

Transformations Among Colloidal Semiconductor Magic-Size Clusters.

A knowledge of colloidal semiconductor magic-size clusters (MSCs) is essential for understanding how fundamental properties evolve during transformations from individual molecules to semiconductor quantum dots (QDs). Compared to QDs, MSCs display much narrower optical absorption bands; the higher cluster stability gives rise to a narrower size distribution. During the production of binary QDs such as II-VI metal (M) chalcogenide (E) ones, binary ME MSCs observed were interpreted as side products and/or the nuclei of QDs.

Ophthalmic Drops with Nanoparticles Derived from a Natural Product for Treating Age-Related Macular Degeneration.

There is a continuing, urgent need for an ophthalmic (eye) drop for the clinical therapy of age-related macular degeneration (AMD), a leading cause of blindness. Here, we report the first formulation of an eye drop that is effective via autophagy for AMD treatment. This eye drop is based on a single natural product derivative (ACD), which is an amphiphilic molecule containing a 6-aminohexanoate group (HN(CH)COO-).

Room-temperature formation of CdS magic-size clusters in aqueous solutions assisted by primary amines.

Aqueous-phase approaches to semiconductor CdS magic-size clusters (MSCs) and the formation pathway have remained relatively unexplored. Here, we report the demonstration of an aqueous-phase, room-temperature approach to CdS MSCs, together with an exploration of their evolution pathway. The resulting CdS MSCs display a sharp optical absorption peak at about 360 nm and are labeled MSC-360.

Room-Temperature Formation Pathway for CdTeSe Alloy Magic-Size Clusters.

Little is known about the pathway of room-temperature formation of ternary CdTeSe magic-size clusters (MSCs) obtained by mixing binary CdTe and CdSe induction period samples containing binary precursor compounds (PCs) of MSCs, monomers (Ms), and fragments (Fs). Also, unestablished are dispersion effects that occur when as-mixed samples (without incubation) are placed in toluene (Tol) and octylamine (OTA) mixtures. The resulting ternary MSCs, exhibiting a sharp optical absorption peak at 399 nm, are labelled CdTeSe MSC-399, and their PCs are referred to as CdTeSe PC-399.

Fragmentation of Magic-Size Cluster Precursor Compounds into Ultrasmall CdS Quantum Dots with Enhanced Particle Yield at Low Temperatures.

Colloidal small-size CdS quantum dots (QDs) are produced usually with low particle yield, together with side products such as the particular precursor compounds (PCs) of magic-size clusters (MSC). Here, we report our synthesis of small-size CdS QDs without the coexistence of the PC and thus with enhanced particle yield. For a conventional reaction of cadmium oleate (Cd(OA) ) and sulfur (S) in 1-octadecene (ODE), we show that after the formation of the PC in the pre-nucleation stage, the addition of tri-n-octylphosphine oxide (TOPO) facilitates the production of small-size QDs.

Evolution of CdTe Magic-Size Clusters with Single Absorption Doublet Assisted by Adding Small Molecules during Prenucleation.

An approach is reported for the exclusive production of CdTe magic-size clusters (MSCs) that exhibit an optical absorption doublet peaking at 385/427 nm, with an explanation of the synthesis procedure. The MSCs, defined as dMSC-427, were produced from the reaction of cadmium oleate (Cd(OA)) and tri--octylphosphine telluride in octadecene at 100 °C, with the addition of acetic acid (HOAc) or acetate (M(OAc)) during the prenucleation stage (40 °C). Without such an addition or when it was performed in the postnucleation stage (100 °C), quantum dots (QDs) developed.

Transformation of ZnS Precursor Compounds to Magic-Size Clusters Exhibiting Optical Absorption Peaking at 269 nm.

We report our investigation on the transformation pathway from precursor compounds (PCs) to magic-size clusters (MSCs) for semiconductor ZnS. We show, for the first time, a synthetic approach to ZnS MSCs in a single-ensemble form exhibiting optical absorption peaking at 269 nm. We thus symbolize the MSCs as MSC-269.

Identifying Clusters and/or Small-Size Quantum Dots in Colloidal CdSe Ensembles with Optical Spectroscopy.

It is well-known that optical absorption and photoluminescence (PL) provide information that is sensitive to the size and size distribution of colloidal binary semiconductor quantum dots (QDs). To explore the nature of reaction products, clusters, and/or small-size QDs, we show that it is important to perform as well photoluminescence excitation (PLE) spectroscopy. For two non-hot-injection reactions of cadmium oleate (Cd(OA)) and selenium (Se) in 1-octadecene (ODE), we show that sequentially extracted products displayed a similar apparent red shift in both absorption and PL with a full width at half-maximum (fwhm) of ∼30 nm.

Four Types of CdTe Magic-Size Clusters from One Prenucleation Stage Sample at Room Temperature.

Four types of colloidal semiconductor CdTe magic-size clusters (MSCs), each of which is in a single-ensemble form, have been obtained at room temperature from a single induction period (IP) sample in dispersion. The induction period is the prenucleation stage that occurs prior to nucleation and growth of colloidal quantum dots (QDs). Three types display sharp optical absorption peaking at either 371, 417, or 448 nm, and the fourth type exhibits a sharp absorption doublet with peaks at 350 and 371 nm.

Photoluminescent Colloidal Nanohelices Self-Assembled from CdSe Magic-Size Clusters via Nanoplatelets.

Reports on photoluminescent colloidal semiconductor two-dimensional (2D) helical nanostructures with one-dimensional quantum confinement are relatively rare. Here, we discuss the formation of such photoluminescent nanostructures for CdSe. We show that when as-synthesized unpurified zero-dimensional (0D) CdSe magic-size clusters (MSCs) (passivated by carboxylate ligands with three-dimensional quantum confinement) are dispersed in a solvent (such as toluene or chloroform) containing hexadecylamine and then subjected to sonication, helical nanostructures are obtained, as observed by transmission electron microscopy.