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      <image:caption>AAV can deliver materials with high efficiency to a wide variety of cell types.</image:caption>
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      <image:title>The Technology - Many scientists believe the key to unlocking CRISPR’s therapeutic potential is delivery via an adeno-associated virus (AAV), an FDA-approved delivery vehicle with a history of safety, efficacy, and lack of toxicity. Until now, the small size of AAV has been a significant obstacle for the packaging of CRISPR, leaving less safe and less effective therapeutic options. To learn more about the CRISPR delivery problem see article from Chemical &amp; Engineering News,</image:title>
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