Ex Parte Breton et alDownload PDFBoard of Patent Appeals and InterferencesJan 18, 201110504906 (B.P.A.I. Jan. 18, 2011) Copy Citation UNITED STATES PATENT AND TRADEMARK OFFICE __________ BEFORE THE BOARD OF PATENT APPEALS AND INTERFERENCES __________ Ex parte LIONEL BRETON, ISABELLE BUREAU-FRANZ, and AUDREY GUENICHE __________ Appeal 2010-000233 Application 10/504,906 Technology Center 1600 __________ Before ERIC GRIMES, MELANIE L. McCOLLUM, and JEFFREY N. FREDMAN, Administrative Patent Judges. McCOLLUM, Administrative Patent Judge. DECISION ON APPEAL1 This is an appeal under 35 U.S.C. § 134 involving claims to a photoprotective composition. The Examiner has rejected the claims as obvious. We have jurisdiction under 35 U.S.C. § 6(b). We affirm. 1 The two-month time period for filing an appeal or commencing a civil action, as recited in 37 C.F.R. § 1.304, or for filing a request for rehearing, as recited in 37 C.F.R. § 41.52, begins to run from the “MAIL DATE” (paper delivery mode) or the “NOTIFICATION DATE” (electronic delivery mode) shown on the PTOL-90A cover letter attached to this decision. Appeal 2010-000233 Application 10/504,906 2 STATEMENT OF THE CASE Claims 1-7, 9, 13, 22-30, and 32-35 are on appeal (App. Br. 4).2 The claims have not been argued separately and therefore stand or fall together. 37 C.F.R. § 41.37(c)(1)(vii). We will focus on claim 1, which reads as follows: 1. An orally administrable photoprotective composition for the photoprotection of the skin, the composition comprising a photoprotecting effective amount of i) at least one probiotic lactic acid bacterium or a culture supernatant thereof, ii) at least one yeast and iii) at least one carotenoid, in an orally acceptable carrier, the lactic acid bacterium present in an amount from about 105 to 1015 cfu/g of the carrier, wherein the carrier is selected from the group consisting of milk, yoghurt, curd, cheese, fermented milks, milk based fermented products, ice-creams, fermented cereal based products, milk based powders, infant formulae and combinations thereof. Claims 1-7, 9, 13, 22-30, and 32-35 stand rejected under 35 U.S.C. § 103(a) as obvious in view of Rivier (US 2003/0059501 A1, Mar. 27, 2003) and De Jong et al. (WO 00/33854 A1, Jun. 15, 2000) (Ans.3 3). The Examiner relies on Rivier for disclosing “an orally administrable composition that comprises a) lactic acid bacterium, b) yeast and c) at least one carotenoid, in an orally acceptable carrier” (id.). The Examiner also finds that Rivier discloses that “the lactic acid bacterium and the yeast can range from 102 to 1012 count/gram” (id.). The Examiner relies on De Jong for teaching “an oral preparation which comprises one or more probiotics”; “that Lactobacillus and Bifidobacterium genera and combinations thereof are preferred suitable 2 Claims 14-21 are also pending but have been withdrawn from consideration (App. Br. 4). 3 “Ans.” refers to the substitute Examiner’s Answer dated June 29, 2009. Appeal 2010-000233 Application 10/504,906 3 probiotics”; “that the yeast strain used in the invention can be of the genus Saccharomyces”; “that it is possible to use both a single microorganism and a mixture of microorganisms”; “that the total concentration of the probiotics is 106 to 1012 live cells per gram of the total product”; and “that the preparation can be in the form of a nutritional supplement, liquid preparation, drinkable liquids, yoghurt, milk, fruit juice, solid or liquid food, tablets, capsules, powders, sachets, pastilles, sweets and bars” (id. at 4). The Examiner finds that “Rivier and De Jong et al. teach analogous inventions related to an orally administrable composition comprising i) at least one probiotic lactic acid bacterium or a culture supernatant thereof, and ii) at least one yeast, in an orally acceptable carrier” (id.). The Examiner concludes that it would have been obvious “to modify the invention of Rivier with the teachings of De Jong et al. because preparing the probiotics in a form disclosed in De Jong et al. will add the beneficial effect of the probiotic reaching the intestine alive and increase optimum action” (id. at 4- 5). Appellants contend that one of ordinary skill in the art would have had no reason to combine Rivier and De Jong because they are directed to unrelated products with different objectives, Rivier teaches away from De Jong, and the proposed combination would change the principles of operation of Rivier and De Jong (App. Br. 11-17; Reply Br. 2-6). ISSUE Does the evidence support the Examiner’s conclusion that it would have been obvious to include a carotenoid, as taught in Rivier, in De Jong’s carrier? Appeal 2010-000233 Application 10/504,906 4 FINDINGS OF FACT 1. The Specification states: “Upon continuous ingestion [of probiotics] by the host they eventually may colonize the gut. . . . Until now a number of different probiotic micro-organisms have been found, which all are reported to exert their effect in the gut.” (Spec. 4: 10-17.) 2. The Specification discloses: It has now been shown that probiotics do also exert an effect in an individual’s body at a location distant from the region in which they colonize it. And particularly, it has been surprisingly found that a composition having a synergistic photoprotective effect on the skin may be obtained by combining into an orally acceptable carrier, a probiotic microorganism and yeast. (Id. at 4: 19-23.) 3. Rivier discloses “a confectionary product that includes at least one functional ingredient” (Rivier, Abstract). 4. As the functional ingredient, Rivier discloses probiotic microorganisms such as Bifidobacterium, Lactobacillus, Streptococcus, or Saccharomyces (id. at ¶ [0042]). 5. Rivier also discloses that antioxidants, including beta-carotene or other carotenoids, “can be used as the functional ingredient, alone or in combination with other functional ingredients” (id. at ¶ [0048]). 6. De Jong discloses a health-promoting preparation containing one or more probiotics (De Jong, Abstract). 7. De Jong also discloses that the probiotics include lactic acid bacteria, yeast strains, or a combination thereof (id. at 3: 18-21). Appeal 2010-000233 Application 10/504,906 5 8. In addition, De Jong discloses that its preparations “can be mixed with a suitable drinkable liquid, such as water, yoghurt, milk, or fruit juice, or can be mixed with solid or liquid food” (id. at 5: 17-19). 9. De Jong also discloses that “[s]uch foods . . . can contain all customary additives for (total and/or clinical) nutrition, including proteins, vitamins, minerals, trace elements and the like” (id. at 5: 31-33). 10. In Example II, De Jong discloses a bar including, among other components, Lb rhamnosus and baker’s yeast (id. at 8: 4-8). PRINCIPLES OF LAW “In order to rely on a reference as a basis for rejection of the applicant’s invention, the reference must either be in the field of the applicant’s endeavor or, if not, then be reasonably pertinent to the particular problem with which the inventor was concerned.” In re Oetiker, 977 F.2d 1443, 1447 (Fed. Cir. 1992). A reference may be said to teach away when a person of ordinary skill, upon reading the reference, would be discouraged from following the path set out in the reference, or would be led in a direction divergent from the path that was taken by the applicant. The degree of teaching away will of course depend on the particular facts; in general, a reference will teach away if it suggests that the line of development flowing from the reference’s disclosure is unlikely to be productive of the result sought by the applicant. In re Gurley, 27 F.3d 551, 553 (Fed. Cir. 1994). A proposed modification or combination of the prior art that would change the basic principles under which the prior art invention was designed to operate weighs against a conclusion of prima facie obviousness. In re Ratti, 270 F.2d 810, 813 (CCPA 1959). Appeal 2010-000233 Application 10/504,906 6 “Mere recognition of latent properties in the prior art does not render nonobvious an otherwise known invention.” In re Baxter Travenol Labs., 952 F.2d 388, 392 (Fed. Cir. 1991). ANALYSIS As with the presently claimed invention, Rivier and De Jong are both related to orally administrable compositions comprising probiotic lactic acid bacterium and/or yeast in an orally acceptable carrier (Findings of Fact (FF) 3-4 & 6-8). Thus, we agree with the Examiner that Rivier and De Jong are analogous art. As noted by Appellants, Rivier relates to a confectionery product (FF 3). However, Appellants have not pointed to, nor did we find, a teaching in Rivier that would have discouraged the use of different types of carriers, such as the ones disclosed in De Jong. Thus, we do not agree with Appellants that Rivier teaches away from using the carriers disclosed in De Jong. According to the Specification, “[i]t has now been shown that probiotics do also exert an effect in an individual’s body at a location distant from the region in which they colonize it,” that is, the gut (FF 1-2 (emphasis added). However, this teaching does not suggest that the probiotics would exert this effect rather than their known effect on the gut. Thus, we do not agree with Appellants that combining De Jong and Rivier to arrive at the present claims would change the principle of operation of De Jong. Instead, we agree with the Examiner that it would have been obvious to include Rivier’s functional ingredients, such as beta-carotene or other carotenoids Appeal 2010-000233 Application 10/504,906 7 (FF 5), in the preparations disclosed in De Jong in order to provide the known benefits of these functional ingredients. CONCLUSION The evidence supports the Examiner’s conclusion that it would have been obvious to include a carotenoid, as taught in Rivier, in De Jong’s carrier. We therefore affirm the obviousness rejection. TIME PERIOD FOR RESPONSE No time period for taking any subsequent action in connection with this appeal may be extended under 37 C.F.R. § 1.136(a). AFFIRMED cdc K&L Gates LLP P.O. Box 1135 CHICAGO, IL 60690 Copy with citationCopy as parenthetical citation