Publications by authors named "Katayoun Saatchi"

Many patients cannot tolerate low-dose weekly methotrexate (MTX) therapy for inflammatory arthritis treatment due to life-threatening toxicity. Although biologics offer a target-specific therapy, it raises the risk of serious infections and even cancer due to immune system suppression. We introduce an anti-inflammatory arthritis MTX ester prodrug using a long-circulating biocompatible polymeric macromolecule: folic acid (FA) functionalized hyperbranched polyglycerol (HPG).

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Human cathelicidin LL-37, a cationic host defense peptide (CHDP), has several important physiological roles, including antimicrobial activity, immune modulation, and wound healing, and is a being investigated as a therapeutic candidate for several indications. While the effects of endogenously produced LL-37 are well studied, the biodistribution of exogenously administered LL-37 are less known. Here we assess the biodistribution of a gallium-67 labeled variant of LL-37 using nuclear imaging techniques over a 48 h period in healthy mice.

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Innate defense regulator-1002 (IDR-1002) is a synthetic peptide with promising immunomodulatory and antibiofilm properties. An appreciable body of work exists around its mechanism of action at the cellular and molecular level, along with its efficacy across several infection and inflammation models. However, little is known about its absorption, distribution, and excretion in live organisms.

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Pretargeting, which is the separation of target accumulation and the administration of a secondary imaging agent into two sequential steps, offers the potential to improve image contrast and reduce radiation burden for nuclear imaging. In recent years, the tetrazine ligation has emerged as a promising approach to facilitate covalent pretargeted imaging due to its unprecedented kinetics and bioorthogonality. Pretargeted bone imaging with TCO-modified alendronic acid (Aln-TCO) is an attractive model that allows the evaluation of tetrazines in healthy animals without the need for complex disease models or targeting regimens.

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  • Frequent use of anti-CD124 monoclonal antibody (αCD124) is common for treating chronic rhinosinusitis with nasal polyps (CRSwNP), and needle-free intranasal delivery is hoped to improve treatment outcomes.
  • Two new nanoconstructs, Nano-P and Dendri-P, were developed to enhance the penetration of αCD124 through nasal tissue, showing better results in mice than traditional methods.
  • These nano-formulations significantly reduced nasal polyps and inflammatory markers without causing toxicity, outperforming higher doses of other delivery methods.
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  • Researchers are exploring the use of external actuation to navigate drug-eluting microrobots in the bloodstream for more targeted drug delivery in cancer treatment.
  • An algorithm was developed to optimize patient positioning based on gravity, enhancing the navigation of magnetic microrobots (MMRs) through the liver arteries in pigs.
  • The results showed a significant increase in the delivery efficiency of MMRs to liver lobes, indicating this technique could improve treatment for patients with liver cancer.
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Persistent pain is a significant healthcare problem with limited treatment options. The high incidence of comorbid chronic pain and depression significantly reduces life quality and complicates the treatment of both conditions. Antidepressants are less effective for pain and depression than for depression alone and they induce severe side effects.

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  • * The study developed a rat model using N1S1 hepatoma cells to better understand tumor growth and test new treatments, observing tumor formation within days and varying tumor take rates across rat types.
  • * Results suggest that immunocompetent SD rats show inconsistent tumor regression, making them unsuitable for therapy research, while immunosuppressed RNU rats provide reliable tumor growth for future investigations.
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Purpose: There is a significant need for a widely available, translatable, sensitive and non-invasive imaging biomarker for tumor hypoxia in radiation oncology. Treatment-induced changes in tumor tissue oxygenation can alter the sensitivity of cancer tissues to radiation, but the relative difficulty in monitoring the tumor microenvironment results in scarce clinical and research data. Oxygen-Enhanced MRI (OE-MRI) uses inhaled oxygen as a contrast agent to measure tissue oxygenation.

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Aptamers are promising targeting agents for imaging and therapy of numerous diseases, including cancer. However, a significant shortcoming of aptamers is their poor stability and fast excretion, limiting their application in vivo. Common strategies to overcome these challenges is to chemically modify aptamers in order to increase their stability and/or to apply formulation technologies such as conjugating them to polymers or nanocarriers in order to increase their circulation half-life.

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Cardiac blood pool imaging is currently performed almost exclusively with Tc-based compounds and SPECT/CT imaging. Using a generator-based PET radioisotope has a few advantages, including not needing nuclear reactors to produce it, obtaining better resolution in humans, and potentially reducing the radiation dose to the patient. When the shortlived radioisotope Ga is used, it can be applied repeatedly on the same day-for example, for the detection of bleeding.

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  • - Peptides are small molecules that play key roles in regulating body functions, but delivering them orally is challenging due to their fragile nature and barriers in the digestive system.
  • - Techniques like protease inhibitors and polymeric encapsulation can help overcome these barriers, but studying their effectiveness using traditional imaging methods is hard due to shallow penetration.
  • - Nuclear imaging emerges as a superior method for tracking how these peptides travel through the gut, offering insights into peptide delivery that connect both peptide science and nuclear medicine.
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Innate defense regulators (IDRs) are synthetic host-defense peptides (HDPs) with broad-spectrum anti-infective properties, including immunomodulatory, anti-biofilm and direct antimicrobial activities. A lack of pharmacokinetic data about these peptides hinders their development and makes it challenging to fully understand how they work in vivo since their mechanism of action is dependent on tissue concentrations of the peptide. Here, we set out to define in detail the pharmacokinetics of a well-characterized IDR molecule, IDR-1018.

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Aptamers are single stranded oligonucleotides that fold into three dimensional structures and are able to recognize a variety of molecular targets. Due to the similarity to antibodies with regards to specificity and affinity and their chemical versatility, aptamers are increasingly used to create targeted probes for molecular imaging and therapy. Hence, aptamer-based probes have been utilized in practically all major imaging modalities such as nuclear imaging, magnetic resonance imaging, x-ray computed tomography, echography and fluorescence imaging, as well as newer modalities such as surface enhanced Raman spectroscopy.

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With the growing interest in developing silver-based antimicrobials, there is a need to better understand the behavior of silver within biological systems. To address this, we showed that single-photon emission computed tomography (SPECT) is a suitable method to noninvasively image Ag-labeled compounds in mice. Formed by neutron irradiation of palladium foil, Ag can be rapidly isolated with a high degree of purity and stably incorporated into antimicrobial silver nanoparticles.

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Objective: Superparamagnetic nanoparticles (SPIONs) can be combined with tumor chemoembolization agents to form magnetic drug-eluting beads (MDEBs), which are navigated magnetically in the MRI scanner through the vascular system. We aim to develop a method to accurately quantify and localize these particles and to validate the method in phantoms and swine models.

Methods: MDEBs were made of FeO SPIONs.

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Human insulin (HI) has fascinating metal-facilitated self-assembly properties that are essential for its biological function. HI has a natural Zn binding site and we have previously shown that covalently attached abiotic ligands (e.g.

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  • Iodine-based X-ray contrast agents (I-XCA) provide better image quality at lower X-ray energies (50-80 kVp), while rhenium-based X-ray contrast agents (Re-XCA) outperform I-XCA at higher energies (above 120 kVp).
  • The study demonstrated that using copper filters enhances the contrast-to-noise ratio (CNR) of Re-XCA significantly, with improvements reaching up to 59.1% at 120 kVp with thicker filters.
  • Monte Carlo simulations indicated that using Re-XCA can reduce the absorbed dose during X-ray imaging while maintaining high-quality images, potentially benefiting medical procedures involving catheters by improving their visibility and placement accuracy.
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Introduction: Magnetic resonance navigation (MRN) uses MRI gradients to steer magnetic drug-eluting beads (MDEBs) across vascular bifurcations. We aim to experimentally verify our theoretical forces balance model (gravitational, thrust, friction, buoyant and gradient steering forces) to improve the MRN targeted success rate.

Method: A single-bifurcation phantom (3 mm inner diameter) made of poly-vinyl alcohol was connected to a cardiac pump at 0.

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  • Albumin is commonly used in the pharmaceutical field to enhance drug effectiveness and reduce toxicity, with macroaggregated albumin (MAA) being one popular format for lung imaging when labeled with technetium-99m.
  • The research introduced a microfluidics platform called microfluidic-MAA (M2A2) that allows for more precise control over the size and uniformity of albumin microparticles, achieving smaller coefficients of variation compared to traditional methods.
  • The M2A2 particles, when labeled with indium-111, showed similar behavior to MAA in animal studies, indicating that this method may improve the development of albumin microparticles for various biomedical applications.
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The validation of metal-phenolic nanoparticles (MPNs) in preclinical imaging studies represents a growing field of interest due to their versatility in forming predesigned structures with unique properties. Before MPNs can be used in medicine, their pharmacokinetics must be optimized so that accumulation in nontargeted organs is prevented and toxicity is minimized. Here, we report the fabrication of MPNs made of a coordination polymer core that combines In(III), Cu(II), and a mixture of the imidazole 1,4-bis(imidazole-1-ylmethyl)-benzene and the catechol 3,4-dihydroxycinnamic acid ligands.

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Due to the increasing inability of antibiotics to treat multidrug-resistant (MDR) bacteria, metal and metal oxide nanoparticles have been gaining interest as antimicrobial agents. Among those, silver nanoparticles have been used extensively as broad-spectrum antimicrobial agents. Here, we describe a newly-developed, 10-min (120 °C at 5 bar pressure) microwave-assisted synthesis of silver nanoparticles made from the wood biopolymer lignin as a reducing and capping agent.

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Pulmonary delivery of small interfering RNA (siRNA)-based drugs is promising in treating severe lung disorders characterized by the upregulated expression of disease-causing genes. Previous studies have shown that the sustained siRNA release can be achieved from polymeric matrix nanoparticles based on poly(lactide--glycolide) (PLGA) loaded with lipoplexes (LPXs) composed of cationic lipid and anionic siRNA (lipid-polymer hybrid nanoparticles, LPNs). Yet, the efficacy, potential for prolonging the pharmacological effect, disposition, and safety of LPNs after pulmonary administration have not been investigated.

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Background: The discovery and development of new medicines requires high-throughput screening of possible therapeutics in a specific model of the disease. Infrared thermal imaging (IRT) is a modern assessment method with extensive clinical and preclinical applications. Employing IRT in longitudinal preclinical setting to monitor arthritis onset, disease activity and therapeutic efficacies requires a standardized framework to provide reproducible quantitative data as a precondition for clinical studies.

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The controlled self-assembly of peptide- and protein-based pharmaceuticals is of central importance for their mode of action and tuning of their properties. Peptide YY (PYY ) is a 36-residue peptide hormone that reduces food intake when peripherally administered. Herein, we describe the synthesis of a PYY analogue functionalized with a metal-ion-binding 2,2'-bipyridine ligand that enables self-assembly through metal complexation.

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