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Injectable Cryogel Vaccine Devices and Methods of Use Thereof

a cryogel and vaccine technology, applied in the direction of vertebrate antigen ingredients, prosthesis, antibody medical ingredients, etc., can solve the problems of high mortality rate, limited efficacy and safety options, and devastating cancers, and achieve the effect of increasing the efficacy of vaccine therapy

Inactive Publication Date: 2018-08-30
PRESIDENT & FELLOWS OF HARVARD COLLEGE
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The invention is about a type of vaccine that is injected into the body to help treat cancer, specifically melanoma and breast cancer. These vaccines are made from a special type of gel that can be quickly and easily prepared, and they are safe and effective. The vaccines also contain cells and other molecules that can help boost the body's immune response. The invention also includes a method for injecting these vaccines using a special tool that can be precise in its delivery. Overall, this invention provides a promising new approach for developing effective cancer vaccines that can protect against disease for a long time.

Problems solved by technology

Cancer is a devastating disease with a high mortality rate that can affect nearly any organ in the body.
Although treatment options exist for certain cancers, these options are limited in terms of efficacy, safety, and applicability to a wide range of cancer types.
However, a major side effect of the surgical implantation of three dimensional scaffolds is the trauma created by physicians while treating patient illness.
In particular, current technologies for the surgical implantation of three dimensional scaffolds involve incisions that lead to patient pain, bleeding, and bruising.

Method used

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  • Injectable Cryogel Vaccine Devices and Methods of Use Thereof
  • Injectable Cryogel Vaccine Devices and Methods of Use Thereof
  • Injectable Cryogel Vaccine Devices and Methods of Use Thereof

Examples

Experimental program
Comparison scheme
Effect test

example 1

e Biodegradable Preformed Macroscopic Geometric Gels

[0204]The compositions and methods described herein provide hydrogels for minimally invasive delivery of shape memory scaffolds for in vivo applications. This method has demonstrated highly efficient and reproducible fabrication of injectable shape-defined macroporous scaffolds. Although only one type of covalently alginate-based crosslinked gel system was evaluated herein, the material performance is readily manipulated by altering its composition, formulation, and degradation profile. The formation of specific shapes and structural stability are desirable characteristics for shape-defined materials, and the most important requirement of these types of materials for minimally invasive therapies is the ability to collapse and faithfully reform the scaffold's structure in a stimulus-responsive manner. A combination of mechanical compression and dehydration is sufficient to compress the scaffolds developed in this work, allowing mini...

example 2

l Integrity of Injectable Macroscopic Shape-Defined Gels

[0206]The deformation of conventional (nanoporous) and macroporous 1% MA-alginate gels under mechanical compression associated with shear forces was examined. Subject to mechanical compression, the gels experience a body of force, which results in a shape change. The influence of the macropores on the gel mechanical properties was also evaluated since the stiffness of the scaffold dictate the extent of the deformation under an applied shear force. Conventional gels give a Young's modulus (i.e., the slope of the initial part of the stress vs. strain curves in FIG. 2) of 42±4 kPa in compression test. However, macroporous gels led to a dramatic reduction in the modulus to 4±2 kPa. As shown in FIG. 2, cylindrical (4 mm diameter×8 mm height) nanoporous gels reduced their heights by ˜16% when subjected to a vertical load before mechanical fracture. In comparison, cylindrical macroporous gels give much larger deformation under lower m...

example 3

ory Injectable Scaffolds As a Controlled Drug Delivery Carrier

[0208]Covalently crosslinked alginate scaffolds possessing shape memory properties were successfully used as a drug delivery system in vivo. The gels having a predefined size and structure were able to exceptionally maintain their structural features after minimally invasive subcutaneously insertion in mice. Suspended gels in PBS were spontaneously hydrated with full geometric restoration after one single injection per site on the lower back of mice. Injected animals did not demonstrate abnormalities in feeding, grooming, or behavior during the time frame of the experiment, nor did they exhibit signs of distress.

[0209]The hydrogels maintained their hydrogel shape integrity at the site of injection. Animal studies performed to examine the integration of the spongy-like gels with the host tissue showed that the alginate-based scaffolds were biocompatible and did not elicit an immune response or rejection when injected in mi...

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PUM

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Abstract

The invention provides polymer compositions for cell and drug delivery.

Description

RELATED APPLICATIONS[0001]This application is continuation of U.S. application Ser. No. 14 / 166,689 filed Jan. 28, 2014, which is a continuation-in-part of U.S. application Ser. No. 14 / 112,096, which is a national stage application, filed under 35 U.S.C. § 371, of International Application No. PCT / US2012 / 035505 filed Apr. 27, 2012, which claims the benefit of priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 61 / 480,237 filed Apr. 28, 2011. This application also claims the benefit of priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 61 / 915,985 filed Dec. 13, 2013 and U.S. Provisional Application No. 61 / 757,509 filed Jan. 28, 2013. The contents of each of these applications are incorporated herein by reference in their entireties.STATEMENT AS TO FEDERALLY SPONSORED RESEARCH[0002]This invention was made with U.S. Government support under Grant Numbers R01 DE013349, 5R01 DE019917-03, and R01 EB015498 from the National Institutes of Health and Award...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K9/70A61K47/42A61K47/36A61K39/00A61L27/56A61L27/54A61L27/50A61L27/26A61K9/00A61K39/39C08L5/04C08L89/06
CPCA61K2039/5152A61K2039/55522A61K9/7007A61L2400/06A61L2300/258A61L2300/252A61L27/56A61L27/54A61L27/50A61K9/0024A61K39/39A61K2039/55561A61L27/26A61K47/42A61K47/36A61K39/0011A61K39/001106A61K39/4611A61K39/4644C08L5/04C08L89/06
Inventor BENCHERIF, SIDI A.SANDS, ROGER WARRENKOSHY, SANDEEP T.MOONEY, DAVID J.
Owner PRESIDENT & FELLOWS OF HARVARD COLLEGE
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