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InQu

InQu® Bone Graft Extender & Substitute

Faster Fusion and Bone Formation

inqu_productfamilyA safe and cost-effective bone graft and substitute, InQu creates a natural micro environment supporting new bone formation in spinal fusions and orthopedic procedures.

The Unmet Need

Surgeons use bone grafts to generate new bone, repair bone defects resulting from trauma and osteotomy, and create spinal fusions. However, using autografts from a patient’s body risks chronic pain and potential infection at the donor site. As a result, surgeons regularly employ a variety of synthetic bone graft substitutes, commonly ceramic and calcium salt-based. Unfortunately, ceramic-based bone grafts lack ideal handling properties and predictable absorption rates.

ISTO’s Solution

InQu was strategically designed as an osteoconductive biosynthetic that provides surgeons with a safe, direct, and rapid path to new bone formation. Unlike other bone graft synthetics, which require a period of mineral breakdown before new bone can begin to form, InQu partners with the body’s natural processes to create new bone in a shorter period of time with no inflammatory response1. InQu is intended for use as a bone graft substitute in the skeletal system (extremities and pelvis) and as a bone graft extender in the spine when combined with bone autograft.

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InQu does not use human or animal cell or tissue, but rather two biomaterials with a long history of safe and effective clinical use2,3,4, InQu interweaves hyaluronic acid (HyA) into the structural support network of resorbable poly(lactide-co-glycolide) (PLGA). This creates a unique microenvironment with an excellent biocompatibility profile that that supports new bone formation and may achieve faster fusion than traditional ceramic bone grafts1.

The unique biosynthetic makeup of InQu has hydrophilic properties, allowing the wicking of blood and other bodily fluids encountered during surgery. Additionally, InQu’s radiolucency allows surgeons to easily distinguish new bone growth on x-ray. InQu’s properties also include excellent compressive resistance similar to that of native trabecular bone5. The rate of InQu resorption and its replacement by newly formed bone is consistent with the rate of bone remodeling at the site of implantation, thus providing the surgeon with predictable results.

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Due to its unique structure, InQu provides surgeons with superior cohesiveness, molding properties, and handling characteristics. InQu is available in three distinct, sterile product configurations (Paste Mix Plus, Matrix, and Granules) to deliver flexibility and ease of use. With its maximum versatility, InQu is appropriate for a variety of spinal and orthopedic procedures.

More Choices. More Versatility.

InQu is offered in three different configurations.


Discover the Advantages of Biosynthetics

  • Superior handling characteristics
  • Unobscured radiographic monitoring of bone healing
  • Predictable resorption

For more information about clinical trial opportunities for InQu or any of our other solutions, please contact ISTO Technologies Customer Service at 1-888-705-ISTO (4786).

To date, InQu has been used in more than 40,000 procedures and has demonstrated an excellent safety profile2.

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InQu Brochure

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Success of Fusion

In a retrospective analysis of 149 spinal fusion procedures, InQu in combination with an autograft demonstrated an overall fusion rate of 93.6% at 12 months7. In a comparative clinical study of InQu vs. tricalcium phosphate in posterolateral spinal fusion, InQu in combination with an autograft achieved a 92.9% successful fusion rate vs. 67.9% for the tricalcium phosphate and autograft group at one year8.

  1. Walsh WR, Oliver RA, Gage G, et al. Application of resorbable poly(lactide-co-glycolide) with entangled hyalauronic acid as an autograft extender for posterolateral intertransverse lumbar fusions in rabbits. Tissue Eng Part A. 2011; 17:213–220. [Epub 2010 Oct 8.]
  2. Athanasiou KA, Niederauer GC, Agrawal CM. Sterilization, toxicity, biocompatibility and clinical applications of polylactic acid/polyglycolic acid copolymers. Biomaterials 1996; 17:93-102.
  3. Theiler R, Bruhlmann P. Overall tolerability and analgesic activity of intra-articular sodium hyaluronate in the treatment of knee osteoarthritis. Curr Med Res Opin 2005; 21:1727-1733.
  4. Novaes AC, Schaiquevich P, Nasswetter G. Multicenter study of hyaluronic acid obtained by biotechnology to evaluate clinical efficacy and safety in knee osteoarthritis. Int J Clin Pharmacol Res 2005; 25:1-7.
  5. Data on file.
  6. Bohner M. Silicon substituted calcium phosphates a critical view. Biomaterials 2009; 30:6403–6406.
  7. Data on file.
  8. Data on file.

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