Ninja Theranostics for overcoming the drug delivery barriers to pediatric brain tumor Project Summary/Abstract Pediatric brain tumors (PBTs) are the leading cause of cancer-related morbidity and mortality among children. Vincristine (VCR) has been approved to treat PBTs, but its inability to cross blood brain barrier (BBB)/blood brain tumor barriers (BBTB) and dose-limiting neuropathy have greatly limited its clinical application. Thus the main challenge is to deliver sufficient amount of drugs to the hard reached PBTs, while multiple barriers including the severe destabilizing condition in the blood, BBB/BBTB, relatively weak enhanced permeability and retention (EPR) effects in brain tumor, and limited uptake in tumor cells should all be taken into consideration to design a whole-process delivery strategy. The goal of this SBIR is to develop a highly effective and less toxic Ninja-type nanoparticle loaded VCR (Ninja-V) against PBTs in preclinical animal models, providing validation regarding the feasibility for Phase II studies that will eventually lead to an IND filing to the FDA. Ninja-V could overcome multi-barriers with several ultimate techniques. It integrates unique stimuli- responsive crosslinking strategy and transformable multistage targeting approach (sequentially targeting BBB/BBTB with glucose transporter as well as tumor cells via overexpressed sialic acid) in a simple one design. This nanoparticle could allow image-guided drug delivery, improve the drug delivery efficacy, and minimize the neurotoxicity. Our hypotheses are: 1) The transformable multistage targeting Ninja-V will be able to cross the BBB/BBTB and facilitate the delivery of encapsulated drugs specifically to PBTs with enhanced tumor cell uptake and deep tissue penetration, thus greatly improving the therapeutic index and minimizing the toxicity. and 2) the Ninja-V consist of stimuli-responsive crosslinkages will minimize premature drug release in blood circulation allow while sparing normal brain tissue and normal organs, and therefore will be more efficacious and less toxic against PBTs compared to the free drug form. State-of-the-art design of nanocarriers via engineering telodendrimers with well-defined structures represents the frontier development of the nanomedicine, in terms of ease of large-scale production, fine-tunable and highly reproducible structure and properties. It will address many translational barriers of nanotherapeutic agents. This simple and unique design of crosslinking and dual targeting nanoparticles with sequential targeting capability, and stimuli-responsive and transformable properties are highly innovative. It is an excellent approach to prevent premature drug release during circulation and deliver high concentrations of drug to tumors. It is expected that this research will lead to a new method for the management of PBTs.
Project Terms: Acids; Active Sites; Address; Affect; Animal Model; Animals; anti-cancer; anticancer activity; base; bench to bedside; Blood; Blood - brain barrier anatomy; Blood Circulation; Brain Neoplasms; brain tissue; Cancer Etiology; cancer therapy; Canis familiaris; Cells; cGMP production; Child; Childhood Brain Neoplasm; childhood cancer mortality; Childhood Central Nervous System Neoplasm; Childhood Malignant Brain Tumor; Cleaved cell; Clinical; clinical application; Companions; Comprehensive Cancer Center; crosslink; Cytotoxic agent; Daunorubicin; design; Deterioration; Development; docetaxel; Dose-Limiting; Doxorubicin; Drug Delivery Systems; Encapsulated; Endocrine; Engineering; Exhibits; experience; FDA approved; first-in-human; Formulation; frontier; Functional disorder; Generations; Glucose; Glucose Transporter; Goals; Growth; Heat-Shock Proteins 90; Histone Deacetylase; Histone Deacetylase Inhibitor; Hydrophobicity; image-guided drug delivery; Impairment; improved; Indocyanine Green; inhibitor/antagonist; innovation; Kyocristine; large scale production; Lead; Liposomes; Malignant Neoplasms; Mediating; Membrane Glycoproteins; Methods; Micelles; Modeling; Morbidity - disease rate; mortality; nanocarrier; nanoformulation; nanomedicine; nanoparticle; nanoparticle drug; nanotheranostics; nanotherapeutic; Neoplasm Metastasis; neoplastic cell; Neuraxis; Neuropathy; Neuropsychology; neurotoxicity; novel; Organ; overexpression; Paclitaxel; Patients; Penetration; Permeability; Pharmaceutical Preparations; Phase; phase 2 study; phase I trial; pilot trial; pre-clinical; premature; Preparation; prevent; Process; Production; Property; Proteasome Inhibitor; Quality of life; Reproducibility; Research; Schools; Sialic Acids; Site; Small Business Innovation Research Grant; SN-38; Solid Neoplasm; Stimulus; Structure; Survival Rate; targeted delivery; Techniques; theranostics; Therapeutic; Therapeutic Index; Tissues; Toxic effect; transcytosis; Translations; tumor; Tumor Tissue; uptake; Validation; Vincristine; Xenograft Model;
