I have been using a RNA clean up kit to improve my A280/260 and A260/30 ratios but the I lost so much RNA, the A260/280 improve and the A60/230 was lower.
It is 8 times lost of your RNA but quality of RNA was improved a lot, you can do two things- first if your requirement is low then proceed with the above protocol secondly if you want a high quantity then just treat your RNA samples with DNase , check on the gel (quality) and use directly for downstream processes.