Appeal No. 2006-2797 Page 13 Application No. 09/341,821 (Fed. Cir. 2006). Here, we find that the nature of the problem – to treat a burn wound – would have suggested to the skilled worker (e.g., a healthcare provider) that Jass’s wound gel bandage requires sterilization, and would have been motivated to accomplish it according to Sperry, as a choice of a conventional technology for accomplishing sterilization. Accordingly, it is our conclusion that claims 9, 19, and 20 are obvious over the combination of Sperry and Jass. Because our reasoning in affirming this rejection differs from the Examiner, we designate it as a new ground of rejection to provide Appellants with a fair opportunity to respond to it. In response to arguments made by Appellants distinguishing Sperry on the basis that it does not teach “dispensing multiple doses,” we concur with the Examiner that Sperry is “relied upon for the solely teaching of the method of making the aerosol.” Answer, Page 10. Other issues Appellants have admitted in their application that barrier aerosol vessels were known in the prior art. Specification, pages 2-4. Upon return of this application to the technology center, we suggest that the Examiner reconsider the prior art as it pertains to claims 5, 6, 10, 14, 15, and 18 and make specific findings on whether any of the prior art barrier aerosol vessels are “self-sealing” and for use with a single composition in contrast to Jass’s teaching. Among the prior art, we call the Examiner’s attention to pages 1680-81 of Remington,4 particularly Fig. 7 which shows a barrier aerosol vessel with a metering valve. 4 Remington: The Science and Practice of Pharmacy, Vol. II, pp. 1680-81 (1995)Page: Previous 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 NextLast modified: November 3, 2007